"PreventionGenetics, part of Exact Sciences"[submitter] AND "GRIP1"[ge - ClinVar

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

Search results

Items: 35

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3029431	NM_001366722.1(GRIP1):c.1260_1261dup	GRIP1	Duplication (3 prime UTR variant)	GRIP1-related disorder	GLikely benign
Select item 310276	NM_001366722.1(GRIP1):c.*1262T>A	GRIP1	Single nucleotide variant (3 prime UTR variant)	Fraser syndrome 3 +1 more	GConflicting classifications of pathogenicity
Select item 707898	NM_001366722.1(GRIP1):c.3369A>T (p.Glu1123Asp)	GRIP1 (E1071D +4 more)	Single nucleotide variant (missense variant)	GRIP1-related disorder +1 more	GLikely benign
Select item 289625	NM_001366722.1(GRIP1):c.3207C>T (p.Pro1069=)	GRIP1	Single nucleotide variant (synonymous variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 1336915	NM_001366722.1(GRIP1):c.2882G>A (p.Arg961Gln)	GRIP1 (R894Q +9 more)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 710021	NM_001366722.1(GRIP1):c.2880G>A (p.Ser960=)	GRIP1	Single nucleotide variant (synonymous variant)	GRIP1-related disorder +2 more	GBenign/Likely benign
Select item 3031385	NM_001366722.1(GRIP1):c.2628A>C (p.Ala876=)	GRIP1	Single nucleotide variant (synonymous variant)	GRIP1-related disorder	GLikely benign
Select item 261411	NM_001366722.1(GRIP1):c.2464+15T>C	GRIP1	Single nucleotide variant (intron variant)	not provided +3 more	GBenign
Select item 2691513	NM_001366722.1(GRIP1):c.2464+3A>G	GRIP1	Single nucleotide variant (intron variant)	GRIP1-related disorder +1 more	GConflicting classifications of pathogenicity
Select item 261410	NM_001366722.1(GRIP1):c.2461C>G (p.Gln821Glu)	GRIP1 (Q769E +3 more)	Single nucleotide variant (missense variant)	not provided +3 more	GBenign
Select item 310304	NM_001366722.1(GRIP1):c.2283G>A (p.Ser761=)	GRIP1	Single nucleotide variant (synonymous variant)	Fraser syndrome 3 +2 more	GBenign/Likely benign
Select item 2868707	NM_001366722.1(GRIP1):c.2001C>T (p.Ser667=)	GRIP1	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 2085623	NM_001366722.1(GRIP1):c.1873G>A (p.Ala625Thr)	GRIP1 (A573T +5 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 261409	NM_001366722.1(GRIP1):c.1838+13G>T	GRIP1	Single nucleotide variant (intron variant)	not provided +3 more	GBenign
Select item 714266	NM_001366722.1(GRIP1):c.1791A>G (p.Gly597=)	GRIP1	Single nucleotide variant (synonymous variant)	GRIP1-related disorder +2 more	GLikely benign
Select item 310306	NM_001366722.1(GRIP1):c.1787C>G (p.Pro596Arg)	GRIP1 (P544R +3 more)	Single nucleotide variant (missense variant)	Fraser syndrome 3 +2 more	GBenign/Likely benign
Select item 2991929	NM_001366722.1(GRIP1):c.1769-10A>G	GRIP1	Single nucleotide variant (intron variant)	not provided +1 more	GLikely benign
Select item 265191	NM_001366722.1(GRIP1):c.1756A>C (p.Ile586Leu)	GRIP1 (I534L +3 more)	Single nucleotide variant (missense variant)	GRIP1-related disorder +3 more	GConflicting classifications of pathogenicity
Select item 381678	NM_001366722.1(GRIP1):c.1645A>G (p.Ile549Val)	GRIP1 (I497V +3 more)	Single nucleotide variant (missense variant)	Fraser syndrome 3 +2 more	GConflicting classifications of pathogenicity
Select item 2887203	NM_001366722.1(GRIP1):c.1452G>T (p.Gly484=)	GRIP1	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 310309	NM_001366722.1(GRIP1):c.1389G>A (p.Gly463=)	GRIP1	Single nucleotide variant (synonymous variant)	Fraser syndrome 3 +2 more	GBenign/Likely benign
Select item 2798103	NM_001366722.1(GRIP1):c.1355-10G>T	GRIP1	Single nucleotide variant (intron variant)	GRIP1-related disorder +1 more	GLikely benign
Select item 3031538	NM_001366722.1(GRIP1):c.1055G>A (p.Arg352Lys)	GRIP1 (R352K +1 more)	Single nucleotide variant (missense variant +1 more)	GRIP1-related disorder	GLikely benign
Select item 2899184	NM_001366722.1(GRIP1):c.873-3T>C	GRIP1	Single nucleotide variant (intron variant)	not provided +1 more	GLikely benign
Select item 2171067	NM_001366722.1(GRIP1):c.867A>C (p.Ala289=)	GRIP1	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 3061683	NM_001366722.1(GRIP1):c.861T>C (p.Ser287=)	GRIP1	Single nucleotide variant (synonymous variant)	GRIP1-related disorder	GLikely benign
Select item 2848838	NM_001366722.1(GRIP1):c.744C>T (p.Ser248=)	GRIP1	Single nucleotide variant (synonymous variant)	GRIP1-related disorder +1 more	GLikely benign
Select item 261413	NM_001366722.1(GRIP1):c.724+10G>A	GRIP1	Single nucleotide variant (intron variant)	not provided +3 more	GBenign
Select item 3051360	NM_001366722.1(GRIP1):c.643A>G (p.Thr215Ala)	GRIP1 (T215A +2 more)	Single nucleotide variant (missense variant)	GRIP1-related disorder	GLikely benign
Select item 261412	NM_001366722.1(GRIP1):c.503-15C>A	GRIP1	Single nucleotide variant (intron variant)	not specified +3 more	GBenign
Select item 2138246	NM_001366722.1(GRIP1):c.418+9A>G	GRIP1	Single nucleotide variant (intron variant)	not provided +1 more	GLikely benign
Select item 2913442	NM_001366722.1(GRIP1):c.273-9A>G	GRIP1	Single nucleotide variant (intron variant)	GRIP1-related disorder +1 more	GBenign/Likely benign
Select item 710172	NM_001366722.1(GRIP1):c.207G>A (p.Ser69=)	GRIP1	Single nucleotide variant (synonymous variant)	GRIP1-related disorder +1 more	GLikely benign
Select item 718093	NM_001366722.1(GRIP1):c.162C>T (p.Val54=)	GRIP1	Single nucleotide variant (synonymous variant)	not provided +2 more	GLikely benign
Select item 3030046	NM_001366723.1(GRIP1):c.56G>C (p.Gly19Ala)	GRIP1 (G19A)	Single nucleotide variant (missense variant +1 more)	GRIP1-related disorder	GBenign

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: 35