Related gene-specific medical variations for Gene (Select 84307) - ClinVar - NCBI

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Items: 18

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3260078	NM_001112734.4(ZSCAN30):c.832A>T (p.Ser278Cys)	ZNF397, ZSCAN30 (S278C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3199437	NM_001112734.4(ZSCAN30):c.1356G>C (p.Gln452His)	ZNF397, ZSCAN30 (Q265H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3199436	NM_001112734.4(ZSCAN30):c.1264T>G (p.Phe422Val)	ZNF397, ZSCAN30 (F235V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3199435	NM_001112734.4(ZSCAN30):c.1238A>G (p.Tyr413Cys)	ZNF397, ZSCAN30 (Y226C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3199434	NM_001112734.4(ZSCAN30):c.1069T>G (p.Tyr357Asp)	ZNF397, ZSCAN30 (Y357D +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2620899	NM_001112734.4(ZSCAN30):c.1343A>T (p.Lys448Ile)	ZNF397, ZSCAN30 (K261I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2550206	NM_001112734.4(ZSCAN30):c.1367T>G (p.Leu456Arg)	ZNF397, ZSCAN30 (L456R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2522711	NM_001112734.4(ZSCAN30):c.1268G>A (p.Gly423Asp)	ZNF397, ZSCAN30 (G236D +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2520243	NM_001112734.4(ZSCAN30):c.869C>G (p.Thr290Arg)	ZNF397, ZSCAN30 (T103R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2512212	NM_001112734.4(ZSCAN30):c.935A>G (p.Gln312Arg)	ZNF397, ZSCAN30 (Q125R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2400016	NM_001112734.4(ZSCAN30):c.1127G>A (p.Arg376Gln)	ZNF397, ZSCAN30 (R376Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2382575	NM_001112734.4(ZSCAN30):c.1301T>C (p.Ile434Thr)	ZNF397, ZSCAN30 (I434T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2376060	NM_001112734.4(ZSCAN30):c.564G>T (p.Met188Ile)	ZSCAN30, ZNF397 (M1I +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2310827	NM_001112734.4(ZSCAN30):c.1187G>A (p.Arg396Gln)	ZNF397, ZSCAN30 (R396Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2306532	NM_001112734.4(ZSCAN30):c.1385T>A (p.Ile462Asn)	ZNF397, ZSCAN30 (I275N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2275150	NM_001112734.4(ZSCAN30):c.1030C>T (p.Leu344Phe)	ZNF397, ZSCAN30 (L157F +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2269076	NM_001112734.4(ZSCAN30):c.842G>T (p.Ser281Ile)	ZNF397, ZSCAN30 (S94I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2223596	NM_001112734.4(ZSCAN30):c.625A>G (p.Met209Val)	ZNF397, ZSCAN30 (M209V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance