ClinVar for Gene (Select 8681) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3307175	NM_001114633.2(PLA2G4B):c.1967G>A (p.Arg656Gln)	JMJD7-PLA2G4B, PLA2G4B (R656Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3287208	NM_005090.4(JMJD7-PLA2G4B):c.1841G>A (p.Arg614Gln)	JMJD7-PLA2G4B, PLA2G4B (R383Q +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3287207	NM_001114632.2(JMJD7):c.805C>G (p.Leu269Val)	JMJD7, JMJD7-PLA2G4B (L269V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3287206	NM_001114632.2(JMJD7):c.904T>A (p.Tyr302Asn)	JMJD7, JMJD7-PLA2G4B (Y302N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3214094	NM_001114633.2(PLA2G4B):c.2257A>C (p.Thr753Pro)	JMJD7-PLA2G4B, PLA2G4B (T984P +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3112414	NM_005090.4(JMJD7-PLA2G4B):c.976G>A (p.Val326Ile)	JMJD7-PLA2G4B, PLA2G4B (V326I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3112413	NM_005090.4(JMJD7-PLA2G4B):c.920T>C (p.Met307Thr)	JMJD7-PLA2G4B, PLA2G4B (M307T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3112412	NM_005090.4(JMJD7-PLA2G4B):c.914A>G (p.Asn305Ser)	JMJD7-PLA2G4B, PLA2G4B (N305S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3112411	NM_005090.4(JMJD7-PLA2G4B):c.892A>G (p.Arg298Gly)	JMJD7-PLA2G4B, PLA2G4B (R67G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3112410	NM_005090.4(JMJD7-PLA2G4B):c.845C>T (p.Thr282Met)	JMJD7-PLA2G4B, PLA2G4B (T51M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3112409	NM_005090.4(JMJD7-PLA2G4B):c.841C>T (p.Arg281Cys)	JMJD7-PLA2G4B, PLA2G4B (R281C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3112408	NM_005090.4(JMJD7-PLA2G4B):c.824G>A (p.Ser275Asn)	JMJD7-PLA2G4B, PLA2G4B (S275N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3112407	NM_005090.4(JMJD7-PLA2G4B):c.794A>G (p.Tyr265Cys)	JMJD7-PLA2G4B, PLA2G4B (Y265C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3112406	NM_005090.4(JMJD7-PLA2G4B):c.779C>T (p.Thr260Ile)	JMJD7-PLA2G4B, PLA2G4B (T260I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3112405	NM_005090.4(JMJD7-PLA2G4B):c.751C>G (p.His251Asp)	JMJD7-PLA2G4B, PLA2G4B (H20D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3112404	NM_005090.4(JMJD7-PLA2G4B):c.34G>C (p.Glu12Gln)	JMJD7, JMJD7-PLA2G4B +1 more (E12Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3112403	NM_005090.4(JMJD7-PLA2G4B):c.3013C>T (p.Arg1005Trp)	JMJD7-PLA2G4B, PLA2G4B (R1005W +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3112402	NM_005090.4(JMJD7-PLA2G4B):c.3008T>G (p.Val1003Gly)	JMJD7-PLA2G4B, PLA2G4B (V772G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3112401	NM_005090.4(JMJD7-PLA2G4B):c.2929G>A (p.Val977Met)	JMJD7-PLA2G4B, PLA2G4B (V977M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3112400	NM_005090.4(JMJD7-PLA2G4B):c.2912C>A (p.Thr971Asn)	JMJD7-PLA2G4B, PLA2G4B (T971N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3112399	NM_005090.4(JMJD7-PLA2G4B):c.2888C>G (p.Ser963Cys)	JMJD7-PLA2G4B, PLA2G4B (S732C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3112398	NM_005090.4(JMJD7-PLA2G4B):c.2852C>T (p.Ala951Val)	JMJD7-PLA2G4B, PLA2G4B (A951V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3112397	NM_005090.4(JMJD7-PLA2G4B):c.2848G>A (p.Glu950Lys)	JMJD7-PLA2G4B, PLA2G4B (E950K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3112396	NM_005090.4(JMJD7-PLA2G4B):c.2774C>T (p.Ala925Val)	JMJD7-PLA2G4B, PLA2G4B (A925V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3112395	NM_005090.4(JMJD7-PLA2G4B):c.2728C>T (p.Arg910Trp)	JMJD7-PLA2G4B, PLA2G4B (R679W +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3112394	NM_005090.4(JMJD7-PLA2G4B):c.2688C>G (p.Phe896Leu)	JMJD7-PLA2G4B, PLA2G4B (F665L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3112393	NM_005090.4(JMJD7-PLA2G4B):c.2684C>T (p.Pro895Leu)	JMJD7-PLA2G4B, PLA2G4B (P664L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3112392	NM_005090.4(JMJD7-PLA2G4B):c.2659C>T (p.Arg887Trp)	JMJD7-PLA2G4B, PLA2G4B (R656W +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3112391	NM_005090.4(JMJD7-PLA2G4B):c.2592C>G (p.Asp864Glu)	JMJD7-PLA2G4B, PLA2G4B (D864E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3112390	NM_005090.4(JMJD7-PLA2G4B):c.2581C>A (p.Pro861Thr)	JMJD7-PLA2G4B, PLA2G4B (P861T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3112389	NM_005090.4(JMJD7-PLA2G4B):c.2513C>T (p.Ser838Leu)	JMJD7-PLA2G4B, PLA2G4B (S838L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3112388	NM_005090.4(JMJD7-PLA2G4B):c.2414T>C (p.Leu805Pro)	JMJD7-PLA2G4B, PLA2G4B (L574P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3112387	NM_005090.4(JMJD7-PLA2G4B):c.2368G>C (p.Asp790His)	JMJD7-PLA2G4B, PLA2G4B (D559H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3112386	NM_005090.4(JMJD7-PLA2G4B):c.2368G>A (p.Asp790Asn)	JMJD7-PLA2G4B, PLA2G4B (D790N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3112385	NM_005090.4(JMJD7-PLA2G4B):c.2322A>G (p.Ile774Met)	JMJD7-PLA2G4B, PLA2G4B (I543M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3112384	NM_005090.4(JMJD7-PLA2G4B):c.2266C>T (p.Arg756Cys)	JMJD7-PLA2G4B, PLA2G4B (R756C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3112383	NM_005090.4(JMJD7-PLA2G4B):c.2260T>A (p.Trp754Arg)	JMJD7-PLA2G4B, PLA2G4B (W523R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3112382	NM_005090.4(JMJD7-PLA2G4B):c.2059G>A (p.Glu687Lys)	JMJD7-PLA2G4B, PLA2G4B (E456K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3112381	NM_005090.4(JMJD7-PLA2G4B):c.2057G>A (p.Cys686Tyr)	JMJD7-PLA2G4B, PLA2G4B (C455Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3112380	NM_005090.4(JMJD7-PLA2G4B):c.2008C>T (p.Leu670Phe)	JMJD7-PLA2G4B, PLA2G4B (L439F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3112379	NM_005090.4(JMJD7-PLA2G4B):c.2008C>G (p.Leu670Val)	JMJD7-PLA2G4B, PLA2G4B (L439V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3112378	NM_005090.4(JMJD7-PLA2G4B):c.1948C>G (p.Leu650Val)	JMJD7-PLA2G4B, PLA2G4B (L650V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3112377	NM_005090.4(JMJD7-PLA2G4B):c.1910A>G (p.Asn637Ser)	JMJD7-PLA2G4B, PLA2G4B (N406S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3112376	NM_005090.4(JMJD7-PLA2G4B):c.1835G>A (p.Arg612Gln)	JMJD7-PLA2G4B, PLA2G4B (R612Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3112375	NM_005090.4(JMJD7-PLA2G4B):c.1834C>T (p.Arg612Trp)	JMJD7-PLA2G4B, PLA2G4B (R381W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3112374	NM_005090.4(JMJD7-PLA2G4B):c.1813C>G (p.Leu605Val)	JMJD7-PLA2G4B, PLA2G4B (L605V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3112373	NM_005090.4(JMJD7-PLA2G4B):c.1807G>A (p.Gly603Ser)	JMJD7-PLA2G4B, PLA2G4B (G603S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3112372	NM_005090.4(JMJD7-PLA2G4B):c.1772A>C (p.Glu591Ala)	JMJD7-PLA2G4B, PLA2G4B (E360A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3112371	NM_005090.4(JMJD7-PLA2G4B):c.1690G>A (p.Gly564Arg)	JMJD7-PLA2G4B, PLA2G4B (G333R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3112370	NM_005090.4(JMJD7-PLA2G4B):c.1686C>G (p.Ile562Met)	JMJD7-PLA2G4B, PLA2G4B (I562M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3112369	NM_005090.4(JMJD7-PLA2G4B):c.1661G>A (p.Gly554Asp)	JMJD7-PLA2G4B, PLA2G4B (G554D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3112368	NM_005090.4(JMJD7-PLA2G4B):c.1612C>T (p.Arg538Trp)	JMJD7-PLA2G4B, PLA2G4B (R307W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3112367	NM_005090.4(JMJD7-PLA2G4B):c.1535A>G (p.Gln512Arg)	JMJD7-PLA2G4B, PLA2G4B (Q512R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3112366	NM_005090.4(JMJD7-PLA2G4B):c.1490C>A (p.Ala497Asp)	JMJD7-PLA2G4B, PLA2G4B (A266D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3112365	NM_005090.4(JMJD7-PLA2G4B):c.1463G>A (p.Gly488Asp)	JMJD7-PLA2G4B, PLA2G4B (G257D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3112363	NM_005090.4(JMJD7-PLA2G4B):c.1324G>A (p.Glu442Lys)	JMJD7-PLA2G4B, PLA2G4B (E211K +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3112362	NM_005090.4(JMJD7-PLA2G4B):c.1284C>G (p.Cys428Trp)	JMJD7-PLA2G4B, PLA2G4B (C428W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3112361	NM_005090.4(JMJD7-PLA2G4B):c.1253C>G (p.Thr418Ser)	JMJD7-PLA2G4B, PLA2G4B (T187S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3112360	NM_005090.4(JMJD7-PLA2G4B):c.1252A>C (p.Thr418Pro)	JMJD7-PLA2G4B, PLA2G4B (T187P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3112359	NM_005090.4(JMJD7-PLA2G4B):c.1171G>A (p.Gly391Arg)	JMJD7-PLA2G4B, PLA2G4B (G391R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3112358	NM_005090.4(JMJD7-PLA2G4B):c.1150C>T (p.His384Tyr)	JMJD7-PLA2G4B, PLA2G4B (H384Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3112357	NM_005090.4(JMJD7-PLA2G4B):c.1133G>A (p.Arg378Gln)	JMJD7-PLA2G4B, PLA2G4B (R147Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3112356	NM_005090.4(JMJD7-PLA2G4B):c.1120G>A (p.Val374Ile)	JMJD7-PLA2G4B, PLA2G4B (V143I +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3112355	NM_005090.4(JMJD7-PLA2G4B):c.1108G>A (p.Val370Ile)	JMJD7-PLA2G4B, PLA2G4B (V139I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3112354	NM_005090.4(JMJD7-PLA2G4B):c.1097G>T (p.Gly366Val)	JMJD7-PLA2G4B, PLA2G4B (G135V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3112353	NM_005090.4(JMJD7-PLA2G4B):c.1019G>A (p.Arg340His)	JMJD7-PLA2G4B, PLA2G4B (R109H +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3112352	NM_005090.4(JMJD7-PLA2G4B):c.1007G>C (p.Gly336Ala)	JMJD7-PLA2G4B, PLA2G4B (G105A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3059773	NM_005090.4(JMJD7-PLA2G4B):c.2748C>T (p.Ser916=)	JMJD7-PLA2G4B, PLA2G4B	Single nucleotide variant (synonymous variant +1 more)	JMJD7-PLA2G4B-related disorder	GBenign
Select item 3059769	NM_005090.4(JMJD7-PLA2G4B):c.1551C>T (p.Asp517=)	JMJD7-PLA2G4B, PLA2G4B	Single nucleotide variant (synonymous variant)	JMJD7-PLA2G4B-related disorder	GBenign
Select item 3059567	NM_005090.4(JMJD7-PLA2G4B):c.1264C>T (p.Arg422Cys)	JMJD7-PLA2G4B, PLA2G4B (R191C +1 more)	Single nucleotide variant (missense variant)	JMJD7-PLA2G4B-related disorder	GBenign
Select item 3059555	NM_005090.4(JMJD7-PLA2G4B):c.2640+5G>A	JMJD7-PLA2G4B, PLA2G4B	Single nucleotide variant (intron variant)	JMJD7-PLA2G4B-related disorder	GBenign
Select item 3058978	NM_005090.4(JMJD7-PLA2G4B):c.2349G>A (p.Arg783=)	JMJD7-PLA2G4B, PLA2G4B	Single nucleotide variant (synonymous variant)	JMJD7-PLA2G4B-related disorder	GBenign
Select item 3057485	NM_005090.4(JMJD7-PLA2G4B):c.1887C>T (p.Phe629=)	JMJD7-PLA2G4B, PLA2G4B	Single nucleotide variant (synonymous variant)	JMJD7-PLA2G4B-related disorder	GLikely benign
Select item 3057053	NM_005090.4(JMJD7-PLA2G4B):c.444C>T (p.Ser148=)	JMJD7, JMJD7-PLA2G4B	Single nucleotide variant (synonymous variant)	JMJD7-PLA2G4B-related disorder	GLikely benign
Select item 3056209	NM_005090.4(JMJD7-PLA2G4B):c.20A>G (p.Glu7Gly)	JMJD7, JMJD7-PLA2G4B +1 more (E7G)	Single nucleotide variant (missense variant)	JMJD7-PLA2G4B-related disorder	GBenign
Select item 3055788	NM_005090.4(JMJD7-PLA2G4B):c.2466A>C (p.Thr822=)	JMJD7-PLA2G4B, PLA2G4B	Single nucleotide variant (synonymous variant)	JMJD7-PLA2G4B-related disorder	GBenign
Select item 3055559	NM_001114632.2(JMJD7):c.779G>A (p.Arg260His)	JMJD7, JMJD7-PLA2G4B (R260H)	Single nucleotide variant (missense variant +1 more)	JMJD7-related disorder	GLikely benign
Select item 3053598	NM_005090.4(JMJD7-PLA2G4B):c.2883G>A (p.Ser961=)	JMJD7-PLA2G4B, PLA2G4B	Single nucleotide variant (synonymous variant +1 more)	JMJD7-PLA2G4B-related disorder	GBenign
Select item 3053479	NM_001114633.2(PLA2G4B):c.382C>T (p.Leu128=)	JMJD7-PLA2G4B, PLA2G4B	Single nucleotide variant (synonymous variant)	PLA2G4B-related disorder	GLikely benign
Select item 3053374	NM_005090.4(JMJD7-PLA2G4B):c.1573-4C>G	JMJD7-PLA2G4B, PLA2G4B	Single nucleotide variant (intron variant)	JMJD7-PLA2G4B-related disorder	GLikely benign
Select item 3052772	NM_001114633.2(PLA2G4B):c.102C>T (p.Tyr34=)	JMJD7-PLA2G4B, PLA2G4B	Single nucleotide variant (synonymous variant)	PLA2G4B-related disorder	GLikely benign
Select item 3052076	NM_005090.4(JMJD7-PLA2G4B):c.2994T>C (p.Ala998=)	JMJD7-PLA2G4B, PLA2G4B	Single nucleotide variant (synonymous variant +1 more)	JMJD7-PLA2G4B-related disorder	GLikely benign
Select item 3050399	NM_005090.4(JMJD7-PLA2G4B):c.2740A>C (p.Thr914Pro)	JMJD7-PLA2G4B, PLA2G4B (T683P +1 more)	Single nucleotide variant (missense variant +1 more)	JMJD7-PLA2G4B-related disorder	GBenign
Select item 3050265	NM_005090.4(JMJD7-PLA2G4B):c.1865G>A (p.Arg622His)	JMJD7-PLA2G4B, PLA2G4B (R391H +1 more)	Single nucleotide variant (missense variant)	JMJD7-PLA2G4B-related disorder	GBenign
Select item 3050244	NM_001114632.2(JMJD7):c.-5C>A	JMJD7, JMJD7-PLA2G4B +1 more	Single nucleotide variant (5 prime UTR variant)	JMJD7-related disorder	GLikely benign
Select item 3050051	NM_005090.4(JMJD7-PLA2G4B):c.2856A>G (p.Ala952=)	JMJD7-PLA2G4B, PLA2G4B (Q890R)	Single nucleotide variant (synonymous variant +1 more)	JMJD7-PLA2G4B-related disorder	GBenign
Select item 3050013	NM_005090.4(JMJD7-PLA2G4B):c.2465C>T (p.Thr822Ile)	JMJD7-PLA2G4B, PLA2G4B (T591I +1 more)	Single nucleotide variant (missense variant)	JMJD7-PLA2G4B-related disorder	GBenign
Select item 3049805	NM_005090.4(JMJD7-PLA2G4B):c.1573-9_1573-7del	JMJD7-PLA2G4B, PLA2G4B	Microsatellite (intron variant)	JMJD7-PLA2G4B-related disorder	GBenign
Select item 3048223	NM_001114633.2(PLA2G4B):c.459C>T (p.His153=)	JMJD7-PLA2G4B, PLA2G4B	Single nucleotide variant (synonymous variant)	PLA2G4B-related disorder	GBenign
Select item 3047744	NM_001114632.2(JMJD7):c.273G>A (p.Ala91=)	JMJD7, JMJD7-PLA2G4B	Single nucleotide variant (synonymous variant)	JMJD7-related disorder	GLikely benign
Select item 3047557	NM_005090.4(JMJD7-PLA2G4B):c.1816G>T (p.Ala606Ser)	JMJD7-PLA2G4B, PLA2G4B (A375S +1 more)	Single nucleotide variant (missense variant)	JMJD7-PLA2G4B-related disorder	GLikely benign
Select item 3047132	NM_005090.4(JMJD7-PLA2G4B):c.1410G>A (p.Met470Ile)	JMJD7-PLA2G4B, PLA2G4B (M239I +1 more)	Single nucleotide variant (missense variant)	JMJD7-PLA2G4B-related disorder	GLikely benign
Select item 3046758	NM_005090.4(JMJD7-PLA2G4B):c.3000C>G (p.Arg1000=)	JMJD7-PLA2G4B, PLA2G4B	Single nucleotide variant (synonymous variant +1 more)	JMJD7-PLA2G4B-related disorder	GLikely benign
Select item 3046306	NM_005090.4(JMJD7-PLA2G4B):c.702+611C>T	JMJD7, JMJD7-PLA2G4B	Single nucleotide variant (3 prime UTR variant +1 more)	JMJD7-PLA2G4B-related disorder	GLikely benign
Select item 3046275	NM_005090.4(JMJD7-PLA2G4B):c.2315T>G (p.Leu772Arg)	JMJD7-PLA2G4B, PLA2G4B (L541R +1 more)	Single nucleotide variant (missense variant)	JMJD7-PLA2G4B-related disorder	GLikely benign
Select item 3045680	NM_005090.4(JMJD7-PLA2G4B):c.1153G>A (p.Val385Ile)	JMJD7-PLA2G4B, PLA2G4B (V154I +1 more)	Single nucleotide variant (missense variant)	JMJD7-PLA2G4B-related disorder	GBenign
Select item 3044931	NM_005090.4(JMJD7-PLA2G4B):c.2710G>A (p.Glu904Lys)	JMJD7-PLA2G4B, PLA2G4B (E673K +1 more)	Single nucleotide variant (missense variant +1 more)	JMJD7-PLA2G4B-related disorder	GLikely benign
Select item 3043749	NM_001114633.2(PLA2G4B):c.982G>A (p.Val328Ile)	JMJD7-PLA2G4B, PLA2G4B (V328I +1 more)	Single nucleotide variant (missense variant)	PLA2G4B-related disorder	GLikely benign
Select item 3043559	NM_005090.4(JMJD7-PLA2G4B):c.1608G>C (p.Gly536=)	JMJD7-PLA2G4B, PLA2G4B	Single nucleotide variant (synonymous variant)	JMJD7-PLA2G4B-related disorder	GLikely benign
Select item 3043511	NM_001114633.2(PLA2G4B):c.83-5C>T	JMJD7-PLA2G4B, PLA2G4B	Single nucleotide variant (intron variant)	PLA2G4B-related disorder	GBenign

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