"ZNF341-related condition"[Disease/phenotype] AND "PreventionGenetics, - ClinVar

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Items: 27

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3042456	NM_001282933.2(ZNF341):c.-7C>T	LOC130065694, ZNF341	Single nucleotide variant (5 prime UTR variant +1 more)	ZNF341-related condition	GBenign
Select item 2635695	NM_001282933.2(ZNF341):c.20A>G (p.Glu7Gly)	LOC130065694, ZNF341 (E7G)	Single nucleotide variant (non-coding transcript variant +2 more)	ZNF341-related condition	GUncertain significance
Select item 1167188	NM_001282933.2(ZNF341):c.150G>T (p.Glu50Asp)	ZNF341 (E50D)	Single nucleotide variant (missense variant +2 more)	ZNF341-related condition +1 more	GBenign/Likely benign
Select item 1166159	NM_001282933.2(ZNF341):c.244G>A (p.Ala82Thr)	ZNF341 (A82T)	Single nucleotide variant (missense variant +2 more)	ZNF341-related condition +1 more	GBenign
Select item 1168992	NM_001282933.2(ZNF341):c.366G>A (p.Pro122=)	ZNF341	Single nucleotide variant (synonymous variant +1 more)	ZNF341-related condition +2 more	GBenign
Select item 1170087	NM_001282933.2(ZNF341):c.479C>T (p.Pro160Leu)	ZNF341 (P160L +1 more)	Single nucleotide variant (missense variant +1 more)	ZNF341-related condition +1 more	GBenign
Select item 1168180	NM_001282933.2(ZNF341):c.553C>T (p.Pro185Ser)	ZNF341 (P185S +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +2 more	GBenign/Likely benign
Select item 1166719	NM_001282933.2(ZNF341):c.672T>C (p.Ala224=)	ZNF341	Single nucleotide variant (synonymous variant +1 more)	ZNF341-related condition +1 more	GBenign/Likely benign
Select item 1600356	NM_001282933.2(ZNF341):c.837C>T (p.Ala279=)	ZNF341	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GBenign/Likely benign
Select item 1986431	NM_001282933.2(ZNF341):c.933G>A (p.Pro311=)	ZNF341	Single nucleotide variant (synonymous variant +2 more)	ZNF341-related condition +1 more	GLikely benign
Select item 1165105	NM_001282933.2(ZNF341):c.1035C>T (p.Thr345=)	ZNF341	Single nucleotide variant (synonymous variant +1 more)	ZNF341-related condition +1 more	GBenign/Likely benign
Select item 1166623	NM_001282933.2(ZNF341):c.1157G>A (p.Arg386Gln)	ZNF341 (R296Q +2 more)	Single nucleotide variant (missense variant +1 more)	ZNF341-related condition +1 more	GBenign
Select item 1627088	NM_001282933.2(ZNF341):c.1248G>A (p.Ala416=)	ZNF341	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign
Select item 1164560	NM_001282933.2(ZNF341):c.1448C>T (p.Thr483Met)	ZNF341 (T393M +2 more)	Single nucleotide variant (missense variant +1 more)	ZNF341-related condition +1 more	GBenign
Select item 1169665	NM_001282933.2(ZNF341):c.1542G>A (p.Ser514=)	ZNF341	Single nucleotide variant (synonymous variant +1 more)	ZNF341-related condition +1 more	GBenign/Likely benign
Select item 1612611	NM_001282933.2(ZNF341):c.1620C>T (p.Tyr540=)	ZNF341	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GBenign/Likely benign
Select item 1167965	NM_001282933.2(ZNF341):c.1622+6T>C	ZNF341	Single nucleotide variant (intron variant)	ZNF341-related condition +1 more	GBenign
Select item 1170037	NM_001282933.2(ZNF341):c.1929C>T (p.Ile643=)	ZNF341, ZNF341-AS1	Single nucleotide variant (synonymous variant +1 more)	ZNF341-related condition +1 more	GBenign
Select item 1169237	NM_001282933.2(ZNF341):c.1932C>T (p.His644=)	ZNF341, ZNF341-AS1	Single nucleotide variant (synonymous variant +1 more)	ZNF341-related condition +1 more	GBenign
Select item 1168952	NM_001282933.2(ZNF341):c.2036-9G>A	ZNF341, ZNF341-AS1	Single nucleotide variant (intron variant)	ZNF341-related condition +1 more	GBenign
Select item 1012482	NM_001282933.2(ZNF341):c.2117C>T (p.Thr706Met)	ZNF341, ZNF341-AS1 (T616M +2 more)	Single nucleotide variant (missense variant +1 more)	Hyper-IgE recurrent infection syndrome 3, autosomal recessive +2 more	GConflicting classifications of pathogenicity
Select item 1167969	NM_001282933.2(ZNF341):c.2148C>T (p.Cys716=)	ZNF341, ZNF341-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GBenign/Likely benign
Select item 1611285	NM_001282933.2(ZNF341):c.2259C>T (p.Pro753=)	ZNF341, ZNF341-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign
Select item 1600415	NM_001282933.2(ZNF341):c.2423C>T (p.Ala808Val)	ZNF341, ZNF341-AS1 (A718V +2 more)	Single nucleotide variant (missense variant +1 more)	ZNF341-related condition +1 more	GBenign
Select item 1164636	NM_001282933.2(ZNF341):c.2437A>C (p.Thr813Pro)	ZNF341, ZNF341-AS1 (T723P +2 more)	Single nucleotide variant (missense variant +1 more)	ZNF341-related condition +1 more	GBenign
Select item 1165798	NM_001282933.2(ZNF341):c.2505T>C (p.Ala835=)	ZNF341, ZNF341-AS1	Single nucleotide variant (synonymous variant +1 more)	ZNF341-related condition +3 more	GBenign
Select item 1589706	NM_001282933.2(ZNF341):c.2532C>T (p.Leu844=)	ZNF341, ZNF341-AS1	Single nucleotide variant (synonymous variant +1 more)	ZNF341-related condition +1 more	GLikely benign

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Items: 27