Related gene-specific medical variations for Gene (Select 81786) - ClinVar

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

Links from Gene

Items: 27

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3328930	NM_203293.3(TRIM7):c.260C>T (p.Pro87Leu)	LOC129995496, TRIM7 (P87L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3328929	NM_203293.3(TRIM7):c.345G>T (p.Glu115Asp)	LOC129995496, TRIM7 (E115D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3328927	NM_203293.3(TRIM7):c.301A>C (p.Thr101Pro)	LOC129995496, TRIM7 (T101P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3328925	NM_203293.3(TRIM7):c.1106G>T (p.Arg369Leu)	TRIM7, TRIM7-AS2 (R161L +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3328924	NM_203293.3(TRIM7):c.1382T>C (p.Val461Ala)	TRIM7, TRIM7-AS2 (V253A +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3328921	NM_203293.3(TRIM7):c.325C>A (p.Pro109Thr)	LOC129995496, TRIM7 (P109T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3328920	NM_203293.3(TRIM7):c.1348C>G (p.Arg450Gly)	TRIM7, TRIM7-AS2 (R450G +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3182781	NM_203293.3(TRIM7):c.236C>A (p.Pro79Gln)	LOC129995496, TRIM7 (P79Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3182780	NM_203293.3(TRIM7):c.1454C>T (p.Thr485Ile)	TRIM7, TRIM7-AS2 (T303I +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3182779	NM_203293.3(TRIM7):c.1360A>C (p.Ser454Arg)	TRIM7, TRIM7-AS2 (S246R +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3182777	NM_203293.3(TRIM7):c.1112A>G (p.Gln371Arg)	TRIM7, TRIM7-AS2 (Q371R +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2606271	NM_203293.3(TRIM7):c.1187G>C (p.Arg396Pro)	TRIM7, TRIM7-AS2 (R214P +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2529534	NM_203293.3(TRIM7):c.1090G>T (p.Val364Leu)	TRIM7, TRIM7-AS2 (V156L +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2528517	NM_203293.3(TRIM7):c.1106G>C (p.Arg369Pro)	TRIM7, TRIM7-AS2 (R161P +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2522404	NM_203293.3(TRIM7):c.1462G>A (p.Val488Ile)	TRIM7, TRIM7-AS2 (V280I +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2517593	NM_203293.3(TRIM7):c.218C>G (p.Pro73Arg)	LOC129995496, TRIM7 (P73R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2516522	NM_203293.3(TRIM7):c.1304T>A (p.Leu435Gln)	TRIM7, TRIM7-AS2 (L435Q +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2481459	NM_203293.3(TRIM7):c.460C>A (p.Arg154Ser)	LOC129995496, TRIM7 (R154S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2477881	NM_203293.3(TRIM7):c.1499T>C (p.Val500Ala)	TRIM7, TRIM7-AS2 (V318A +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2467991	NM_203293.3(TRIM7):c.1418C>T (p.Ser473Phe)	TRIM7, TRIM7-AS2 (S265F +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2464179	NM_203293.3(TRIM7):c.278A>C (p.Asn93Thr)	LOC129995496, TRIM7 (N93T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2402529	NM_203293.3(TRIM7):c.302C>G (p.Thr101Arg)	LOC129995496, TRIM7 (T101R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2351326	NM_203293.3(TRIM7):c.481C>G (p.His161Asp)	LOC129995496, TRIM7 (H161D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2298293	NM_203293.3(TRIM7):c.1472A>G (p.Gln491Arg)	TRIM7, TRIM7-AS2 (Q309R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2294698	NM_203293.3(TRIM7):c.244C>T (p.Arg82Cys)	LOC129995496, TRIM7 (R82C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2205449	NM_203293.3(TRIM7):c.388T>A (p.Cys130Ser)	LOC129995496, TRIM7 (C130S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2205448	NM_203293.3(TRIM7):c.376G>T (p.Ala126Ser)	LOC129995496, TRIM7 (A126S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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: 27