Related gene-specific medical variations for Gene (Select 650669) - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Links from Gene

Items: 68

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3280809	NM_000820.4(GAS6):c.823G>A (p.Asp275Asn)	GAS6, GAS6-AS1 (D275N)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3280808	NM_000820.4(GAS6):c.428T>C (p.Leu143Pro)	GAS6, GAS6-AS1 (L143P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280806	NM_000820.4(GAS6):c.1168A>C (p.Asn390His)	GAS6, GAS6-AS1 (N390H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280805	NM_000820.4(GAS6):c.1750G>T (p.Gly584Cys)	GAS6, GAS6-AS1 (G584C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3098674	NM_000820.4(GAS6):c.946C>G (p.Pro316Ala)	GAS6, GAS6-AS1 (P316A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3098672	NM_000820.4(GAS6):c.789C>G (p.Asp263Glu)	GAS6, GAS6-AS1 (D263E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3098671	NM_000820.4(GAS6):c.718G>A (p.Asp240Asn)	GAS6, GAS6-AS1 (D240N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3098670	NM_000820.4(GAS6):c.710G>C (p.Arg237Pro)	GAS6, GAS6-AS1 (R237P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3098669	NM_000820.4(GAS6):c.692C>A (p.Ser231Tyr)	GAS6, GAS6-AS1 (S231Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3098668	NM_000820.4(GAS6):c.617C>T (p.Ala206Val)	GAS6, GAS6-AS1 (A206V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3098667	NM_000820.4(GAS6):c.559G>A (p.Glu187Lys)	GAS6, GAS6-AS1 (E187K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3098666	NM_000820.4(GAS6):c.460G>C (p.Asp154His)	GAS6, GAS6-AS1 (D154H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3098665	NM_000820.4(GAS6):c.395C>T (p.Ala132Val)	GAS6, GAS6-AS1 (A132V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3098664	NM_000820.4(GAS6):c.1943T>G (p.Val648Gly)	GAS6, GAS6-AS1 (V648G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3098663	NM_000820.4(GAS6):c.1769T>C (p.Val590Ala)	GAS6, GAS6-AS1 (V590A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3098662	NM_000820.4(GAS6):c.1765G>C (p.Glu589Gln)	GAS6, GAS6-AS1 (E589Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3098661	NM_000820.4(GAS6):c.1715G>A (p.Gly572Asp)	GAS6, GAS6-AS1 (G572D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3098660	NM_000820.4(GAS6):c.1495G>A (p.Val499Ile)	GAS6, GAS6-AS1 (V499I)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3098659	NM_000820.4(GAS6):c.1415C>T (p.Ser472Leu)	GAS6, GAS6-AS1 (S472L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3098658	NM_000820.4(GAS6):c.1216G>A (p.Ala406Thr)	GAS6, GAS6-AS1 (A406T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3098657	NM_000820.4(GAS6):c.1213G>A (p.Val405Met)	GAS6, GAS6-AS1 (V405M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3098656	NM_000820.4(GAS6):c.1166G>A (p.Arg389Gln)	GAS6, GAS6-AS1 (R389Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3098655	NM_000820.4(GAS6):c.1153G>A (p.Glu385Lys)	GAS6, GAS6-AS1 (E385K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3098654	NM_000820.4(GAS6):c.1093G>A (p.Gly365Ser)	GAS6, GAS6-AS1 (G365S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3098653	NM_000820.4(GAS6):c.1078C>T (p.Arg360Cys)	GAS6, GAS6-AS1 (R360C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2611099	NM_000820.4(GAS6):c.1640A>C (p.Lys547Thr)	GAS6, GAS6-AS1 (K547T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2593302	NM_000820.4(GAS6):c.1912G>A (p.Ala638Thr)	GAS6, GAS6-AS1 (A638T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2553836	NM_000820.4(GAS6):c.1384G>A (p.Val462Met)	GAS6, GAS6-AS1 (V462M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2543244	NM_000820.4(GAS6):c.672C>G (p.Asp224Glu)	GAS6, GAS6-AS1 (D224E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2530859	NM_000820.4(GAS6):c.497G>A (p.Gly166Asp)	GAS6, GAS6-AS1 (G166D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2530126	NM_000820.4(GAS6):c.2015C>T (p.Pro672Leu)	GAS6-AS1, GAS6 (P672L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2520080	NM_000820.4(GAS6):c.1432T>G (p.Ser478Ala)	GAS6, GAS6-AS1 (S478A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2508053	NM_000820.4(GAS6):c.1591C>T (p.Arg531Cys)	GAS6, GAS6-AS1 (R531C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2401654	NM_000820.4(GAS6):c.1111G>A (p.Gly371Ser)	GAS6, GAS6-AS1 (G371S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2379651	NM_000820.4(GAS6):c.1168A>G (p.Asn390Asp)	GAS6, GAS6-AS1 (N390D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2372899	NM_000820.4(GAS6):c.1421C>T (p.Thr474Met)	GAS6, GAS6-AS1 (T474M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2370085	NM_000820.4(GAS6):c.410T>C (p.Met137Thr)	GAS6, GAS6-AS1 (M137T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2368903	NM_000820.4(GAS6):c.997A>G (p.Ile333Val)	GAS6, GAS6-AS1 (I333V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2353518	NM_000820.4(GAS6):c.850G>A (p.Val284Met)	GAS6, GAS6-AS1 (V284M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2341472	NM_000820.4(GAS6):c.1828G>A (p.Val610Met)	GAS6, GAS6-AS1 (V610M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2320135	NM_000820.4(GAS6):c.362C>T (p.Thr121Met)	GAS6, GAS6-AS1 (T121M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2318934	NM_000820.4(GAS6):c.1322T>C (p.Leu441Pro)	GAS6, GAS6-AS1 (L441P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2297348	NM_000820.4(GAS6):c.1690C>A (p.Leu564Ile)	GAS6, GAS6-AS1 (L564I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2292992	NM_000820.4(GAS6):c.797G>A (p.Gly266Glu)	GAS6, GAS6-AS1 (G266E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2278938	NM_000820.4(GAS6):c.1625A>G (p.Tyr542Cys)	GAS6, GAS6-AS1 (Y542C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2274798	NM_000820.4(GAS6):c.790G>A (p.Gly264Arg)	GAS6, GAS6-AS1 (G264R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2270653	NM_000820.4(GAS6):c.1720G>A (p.Glu574Lys)	GAS6, GAS6-AS1 (E574K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2264306	NM_000820.4(GAS6):c.460G>A (p.Asp154Asn)	GAS6, GAS6-AS1 (D154N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2260405	NM_000820.4(GAS6):c.794G>T (p.Arg265Leu)	GAS6, GAS6-AS1 (R265L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2253366	NM_000820.4(GAS6):c.827C>T (p.Thr276Ile)	GAS6, GAS6-AS1 (T276I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2251356	NM_000820.4(GAS6):c.1457C>T (p.Ala486Val)	GAS6, GAS6-AS1 (A486V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2248059	NM_000820.4(GAS6):c.731A>C (p.Gln244Pro)	GAS6, GAS6-AS1 (Q244P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2237625	NM_000820.4(GAS6):c.1427G>A (p.Arg476Lys)	GAS6, GAS6-AS1 (R476K)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2236853	NM_000820.4(GAS6):c.1592G>A (p.Arg531His)	GAS6, GAS6-AS1 (R531H)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2217073	NM_000820.4(GAS6):c.1792G>A (p.Glu598Lys)	GAS6, GAS6-AS1 (E598K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2214412	NM_000820.4(GAS6):c.1870G>A (p.Gly624Ser)	GAS6, GAS6-AS1 (G624S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 791331	NM_000820.4(GAS6):c.1321C>T (p.Leu441=)	GAS6, GAS6-AS1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 791330	NM_000820.4(GAS6):c.1498G>A (p.Gly500Arg)	GAS6, GAS6-AS1 (G500R)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 787414	NM_000820.4(GAS6):c.1847G>A (p.Arg616Gln)	GAS6, GAS6-AS1 (R616Q)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 786243	NM_000820.4(GAS6):c.1834G>A (p.Glu612Lys)	GAS6, GAS6-AS1 (E612K)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 781125	NM_000820.4(GAS6):c.1739C>T (p.Ser580Leu)	GAS6, GAS6-AS1 (S580L)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 768636	NM_000820.4(GAS6):c.1497C>T (p.Val499=)	GAS6, GAS6-AS1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 759955	NM_000820.4(GAS6):c.1902G>A (p.Ala634=)	GAS6, GAS6-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 741682	NM_000820.4(GAS6):c.816G>A (p.Gln272=)	GAS6, GAS6-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 731365	NM_000820.4(GAS6):c.1791C>T (p.Ser597=)	GAS6, GAS6-AS1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 722726	NM_000820.4(GAS6):c.835-8C>T	GAS6, GAS6-AS1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 713018	NM_000820.4(GAS6):c.683C>T (p.Ala228Val)	GAS6-AS1, GAS6 (A228V)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 713017	NM_000820.4(GAS6):c.1883-3C>T	GAS6, GAS6-AS1	Single nucleotide variant (intron variant)	not provided	GLikely benign

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Links from Gene

Items: 68