"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "VARS1"[gen - ClinVar

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

Search results

Items: 29

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2656418	NM_006295.3(VARS1):c.3591T>G (p.Pro1197=)	VARS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2656419	NM_006295.3(VARS1):c.3579G>A (p.Gly1193=)	VARS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 774865	NM_006295.3(VARS1):c.3459C>T (p.Tyr1153=)	VARS1	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 2571247	NM_006295.3(VARS1):c.3432C>T (p.Gly1144=)	VARS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2656420	NM_006295.3(VARS1):c.3417G>A (p.Ala1139=)	VARS1	Single nucleotide variant (synonymous variant)	VARS1-related condition +1 more	GLikely benign
Select item 2656421	NM_006295.3(VARS1):c.3346C>A (p.Arg1116=)	VARS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2656422	NM_006295.3(VARS1):c.3336A>G (p.Leu1112=)	VARS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1299022	NM_006295.3(VARS1):c.3318C>T (p.Ala1106=)	VARS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 559443	NM_006295.3(VARS1):c.3214T>C (p.Phe1072Leu)	VARS1 (F1072L)	Single nucleotide variant (missense variant)	not provided +7 more	GConflicting classifications of pathogenicity
Select item 2656423	NM_006295.3(VARS1):c.3162C>T (p.Asp1054=)	VARS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 932466	NM_006295.3(VARS1):c.2687C>G (p.Pro896Arg)	VARS1 (P896R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3026783	NM_006295.3(VARS1):c.2272C>A (p.Arg758Ser)	VARS1 (R758S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 785163	NM_006295.3(VARS1):c.2073C>T (p.Ala691=)	VARS1	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 2656424	NM_006295.3(VARS1):c.1998G>A (p.Ser666=)	VARS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2656425	NM_006295.3(VARS1):c.1878G>A (p.Pro626=)	VARS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1695154	NM_006295.3(VARS1):c.1853G>A (p.Arg618Gln)	VARS1 (R618Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 1219611	NM_006295.3(VARS1):c.1843A>G (p.Met615Val)	VARS1 (M615V)	Single nucleotide variant (missense variant)	not provided	GConflicting classifications of pathogenicity
Select item 2656426	NM_006295.3(VARS1):c.1701A>G (p.Pro567=)	VARS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2499000	NM_006295.3(VARS1):c.1696C>T (p.His566Tyr)	VARS1 (H566Y)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1335620	NM_006295.3(VARS1):c.1610G>A (p.Arg537Gln)	VARS1 (R537Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 781866	NM_006295.3(VARS1):c.1413T>C (p.Ser471=)	VARS1	Single nucleotide variant (synonymous variant)	VARS1-related condition +1 more	GBenign/Likely benign
Select item 2656427	NM_006295.3(VARS1):c.1389C>T (p.His463=)	VARS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 562000	NM_006295.3(VARS1):c.1210C>T (p.Arg404Trp)	VARS1 (R404W)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 708429	NM_006295.3(VARS1):c.858C>T (p.Pro286=)	LOC126859651, VARS1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2656428	NM_006295.3(VARS1):c.579G>A (p.Thr193=)	LOC126859651, VARS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 708430	NM_006295.3(VARS1):c.542G>A (p.Arg181His)	LOC126859651, VARS1 (R181H)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 708431	NM_006295.3(VARS1):c.523-3del	LOC126859651, VARS1	Deletion (intron variant)	not provided	GBenign
Select item 3025324	NM_006295.3(VARS1):c.135C>T (p.Pro45=)	VARS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 624231	NM_006295.3(VARS1):c.47T>G (p.Leu16Arg)	VARS1 (L16R)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Search results

Items: 29