ClinVar for Gene (Select 10274) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3251800	NM_005862.3(STAG1):c.471+6G>A	STAG1	Single nucleotide variant (intron variant)	not specified	GUncertain significance
Select item 3251372	NM_005862.3(STAG1):c.3066-16del	STAG1	Deletion (intron variant)	not specified	GLikely benign
Select item 3235830	NM_005862.3(STAG1):c.1706A>T (p.Glu569Val)	STAG1 (E569V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3235773	NM_005862.3(STAG1):c.1159T>C (p.Tyr387His)	STAG1 (Y387H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3170872	NM_005862.3(STAG1):c.967A>G (p.Ser323Gly)	STAG1 (S323G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3170871	NM_005862.3(STAG1):c.85A>G (p.Thr29Ala)	STAG1 (T29A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3170869	NM_005862.3(STAG1):c.3385A>G (p.Met1129Val)	STAG1 (M1129V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3170868	NM_005862.3(STAG1):c.3380G>A (p.Arg1127Gln)	STAG1 (R1127Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 3069050	NM_005862.3(STAG1):c.3435C>T (p.Asp1145=)	STAG1	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3069049	NM_005862.3(STAG1):c.471+14A>G	STAG1	Single nucleotide variant (intron variant)	not specified	GLikely benign
Select item 3063925	NM_005862.3(STAG1):c.2371-8T>C	STAG1	Single nucleotide variant (intron variant)	not specified	GUncertain significance
Select item 3062729	GRCh37/hg19 3q22.3(chr3:136325960-136530649)x3	STAG1	Copy number gain	not specified	GUncertain significance
Select item 3062171	NM_005862.3(STAG1):c.2099C>T (p.Ser700Phe)	STAG1 (S700F)	Single nucleotide variant (missense variant)	See cases	GUncertain significance
Select item 3040551	NM_005862.3(STAG1):c.2550T>C (p.Gly850=)	STAG1	Single nucleotide variant (synonymous variant)	STAG1-related disorder	GLikely benign
Select item 3036309	NM_005862.3(STAG1):c.3312C>A (p.Thr1104=)	STAG1	Single nucleotide variant (synonymous variant)	STAG1-related disorder	GLikely benign
Select item 3031406	NM_005862.3(STAG1):c.3271+5G>A	STAG1	Single nucleotide variant (intron variant)	STAG1-related disorder	GUncertain significance
Select item 3029601	NM_005862.3(STAG1):c.3003G>A (p.Leu1001=)	STAG1	Single nucleotide variant (synonymous variant)	STAG1-related disorder	GLikely benign
Select item 3027404	GRCh37/hg19 3q22.3(chr3:136219065-136365036)x1	STAG1	Copy number loss	not provided	GPathogenic
Select item 3021221	NM_005862.3(STAG1):c.3364C>T (p.Leu1122=)	STAG1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3016736	NM_005862.3(STAG1):c.741C>T (p.Thr247=)	STAG1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3013656	NM_005862.3(STAG1):c.152G>A (p.Arg51Gln)	STAG1 (R51Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3013049	NM_005862.3(STAG1):c.1026+9C>G	STAG1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3010608	NM_005862.3(STAG1):c.2134C>G (p.Leu712Val)	STAG1 (L712V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3000157	NM_005862.3(STAG1):c.750A>G (p.Gln250=)	STAG1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2912924	NM_005862.3(STAG1):c.471+7C>T	STAG1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2912252	NM_005862.3(STAG1):c.1546+10T>A	STAG1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2907482	NM_005862.3(STAG1):c.1461T>C (p.Ser487=)	STAG1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2903254	NM_005862.3(STAG1):c.1744-5_1744-3del	STAG1	Deletion (intron variant)	not provided	GLikely benign
Select item 2899544	NM_005862.3(STAG1):c.223C>G (p.His75Asp)	STAG1 (H75D)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2894975	NM_005862.3(STAG1):c.1273C>T (p.Arg425Cys)	STAG1 (R425C)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2894768	NM_005862.3(STAG1):c.3033T>A (p.Ser1011=)	STAG1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2890075	NM_005862.3(STAG1):c.1278T>G (p.Pro426=)	STAG1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2889591	NM_005862.3(STAG1):c.472-9G>A	STAG1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2889503	NM_005862.3(STAG1):c.2165C>T (p.Thr722Ile)	STAG1 (T722I)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2888283	NM_005862.3(STAG1):c.1744-5T>C	STAG1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2887883	NM_005862.3(STAG1):c.37A>G (p.Thr13Ala)	STAG1 (T13A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2881731	NM_005862.3(STAG1):c.2197-17T>C	STAG1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2881196	NM_005862.3(STAG1):c.549A>C (p.Gly183=)	STAG1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2881071	NM_005862.3(STAG1):c.2188C>G (p.Pro730Ala)	STAG1 (P730A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2880588	NM_005862.3(STAG1):c.1867G>A (p.Val623Ile)	STAG1 (V623I)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2879395	NM_005862.3(STAG1):c.1204C>T (p.His402Tyr)	STAG1 (H402Y)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2878918	NM_005862.3(STAG1):c.1335A>T (p.Pro445=)	STAG1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2878333	NM_005862.3(STAG1):c.2788-13_2788-12dup	STAG1	Duplication (intron variant)	not provided	GBenign
Select item 2878209	NM_005862.3(STAG1):c.2409C>T (p.Ser803=)	STAG1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2877343	NM_005862.3(STAG1):c.3483G>A (p.Lys1161=)	STAG1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2877336	NM_005862.3(STAG1):c.2223C>T (p.Ser741=)	STAG1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2877040	NM_005862.3(STAG1):c.791A>G (p.Asn264Ser)	STAG1 (N264S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2876785	NM_005862.3(STAG1):c.204C>T (p.Gly68=)	STAG1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2876397	NM_005862.3(STAG1):c.2686-12T>C	STAG1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2875946	NM_005862.3(STAG1):c.3192C>T (p.Asn1064=)	STAG1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2875209	NM_005862.3(STAG1):c.2277+15C>G	STAG1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2874245	NM_005862.3(STAG1):c.1339G>A (p.Ala447Thr)	STAG1 (A447T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2873734	NM_005862.3(STAG1):c.2185A>C (p.Met729Leu)	STAG1 (M729L)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2872646	NM_005862.3(STAG1):c.1081A>C (p.Arg361=)	STAG1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2872413	NM_005862.3(STAG1):c.2184C>T (p.Ala728=)	STAG1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2872247	NM_005862.3(STAG1):c.1651-14G>A	STAG1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2871968	NM_005862.3(STAG1):c.1547-8T>C	STAG1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2871873	NM_005862.3(STAG1):c.676+14A>G	STAG1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2871334	NM_005862.3(STAG1):c.2292A>G (p.Val764=)	STAG1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2871145	NM_005862.3(STAG1):c.3564T>C (p.Gly1188=)	STAG1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2870951	NM_005862.3(STAG1):c.2546-17T>G	STAG1	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2870858	NM_005862.3(STAG1):c.1074T>C (p.Tyr358=)	STAG1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2870855	NM_005862.3(STAG1):c.2724G>C (p.Leu908=)	STAG1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2870766	NM_005862.3(STAG1):c.3313A>G (p.Met1105Val)	STAG1 (M1105V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2870524	NM_005862.3(STAG1):c.903-19C>G	STAG1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2870001	NM_005862.3(STAG1):c.394+5A>G	STAG1	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2869316	NM_005862.3(STAG1):c.2478A>G (p.Gln826=)	STAG1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2869200	NM_005862.3(STAG1):c.3750_3751inv (p.Asp1250_Ser1251delinsGluThr)	STAG1	Inversion (missense variant)	not provided	GUncertain significance
Select item 2869176	NM_005862.3(STAG1):c.2788-19_2788-17del	STAG1	Microsatellite (intron variant)	not provided	GLikely benign
Select item 2869069	NM_005862.3(STAG1):c.1027-7del	STAG1	Deletion (intron variant)	not provided	GLikely benign
Select item 2868546	NM_005862.3(STAG1):c.3368G>A (p.Arg1123Gln)	STAG1 (R1123Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2868465	NM_005862.3(STAG1):c.676+14A>T	STAG1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2868425	NM_005862.3(STAG1):c.1125+16_1125+18del	STAG1	Deletion (intron variant)	not provided	GLikely benign
Select item 2868252	NM_005862.3(STAG1):c.2545+19T>C	STAG1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2867967	NM_005862.3(STAG1):c.829-20T>C	STAG1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2866995	NM_005862.3(STAG1):c.3215C>A (p.Thr1072Asn)	STAG1 (T1072N)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2866714	NM_005862.3(STAG1):c.46A>T (p.Thr16Ser)	STAG1 (T16S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2862823	NM_005862.3(STAG1):c.3446+14A>T	STAG1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2862143	NM_005862.3(STAG1):c.2197-11A>G	STAG1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2861818	NM_005862.3(STAG1):c.3065+10A>G	STAG1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2860581	NM_005862.3(STAG1):c.29+12A>G	STAG1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2857082	NM_005862.3(STAG1):c.1206-13C>G	STAG1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2856848	NM_005862.3(STAG1):c.1429-6T>C	STAG1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2839264	NM_005862.3(STAG1):c.902+9T>C	STAG1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2834913	NM_005862.3(STAG1):c.1611T>C (p.Ala537=)	STAG1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2820854	NM_005862.3(STAG1):c.1205+18C>G	STAG1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2820489	NM_005862.3(STAG1):c.2445G>T (p.Gln815His)	STAG1 (Q815H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2814955	NM_005862.3(STAG1):c.934A>G (p.Ile312Val)	STAG1 (I312V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2813830	NM_005862.3(STAG1):c.1668A>C (p.Glu556Asp)	STAG1 (E556D)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2813514	NM_005862.3(STAG1):c.1551G>A (p.Met517Ile)	STAG1 (M517I)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2812549	NM_005862.3(STAG1):c.2818C>A (p.Pro940Thr)	STAG1 (P940T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2808131	NM_005862.3(STAG1):c.524G>T (p.Arg175Leu)	STAG1 (R175L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2803225	NM_005862.3(STAG1):c.3692G>A (p.Arg1231Gln)	STAG1 (R1231Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2801431	NM_005862.3(STAG1):c.3159C>T (p.Val1053=)	STAG1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2797497	NM_005862.3(STAG1):c.2545+13A>G	STAG1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2797201	NM_005862.3(STAG1):c.1026+13G>C	STAG1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2796379	NM_005862.3(STAG1):c.2280G>A (p.Glu760=)	STAG1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2795642	NM_005862.3(STAG1):c.136A>G (p.Thr46Ala)	STAG1 (T46A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2794759	NM_005862.3(STAG1):c.2685+19A>G	STAG1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2792152	NM_005862.3(STAG1):c.2673A>G (p.Lys891=)	STAG1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign

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