"PreventionGenetics, part of Exact Sciences"[submitter] AND "ARSG"[gen - ClinVar

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Items: 21

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 769924	NM_001267727.2(ARSG):c.32C>T (p.Ala11Val)	ARSG (A11V)	Single nucleotide variant (missense variant)	ARSG-related condition +1 more	GBenign
Select item 708031	NM_001267727.2(ARSG):c.87G>A (p.Gly29=)	ARSG	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 1159842	NM_001267727.2(ARSG):c.360C>T (p.Thr120=)	ARSG	Single nucleotide variant (synonymous variant)	ARSG-related condition +1 more	GLikely benign
Select item 1021538	NM_001267727.2(ARSG):c.396T>A (p.Thr132=)	ARSG	Single nucleotide variant (synonymous variant)	ARSG-related condition +1 more	GLikely benign
Select item 1540483	NM_001267727.2(ARSG):c.507T>C (p.Asp169=)	ARSG	Single nucleotide variant (synonymous variant)	ARSG-related condition +1 more	GLikely benign
Select item 1169241	NM_001267727.2(ARSG):c.595G>A (p.Val199Met)	ARSG (V183M +1 more)	Single nucleotide variant (missense variant)	ARSG-related condition +1 more	GBenign
Select item 768914	NM_001267727.2(ARSG):c.603C>T (p.Leu201=)	ARSG	Single nucleotide variant (synonymous variant)	ARSG-related condition +1 more	GBenign/Likely benign
Select item 1085772	NM_001267727.2(ARSG):c.711C>T (p.Ser237=)	ARSG	Single nucleotide variant (synonymous variant)	ARSG-related condition +1 more	GLikely benign
Select item 2995732	NM_001267727.2(ARSG):c.723C>T (p.Phe241=)	ARSG	Single nucleotide variant (synonymous variant)	ARSG-related condition +1 more	GLikely benign
Select item 787600	NM_001267727.2(ARSG):c.786G>A (p.Ala262=)	ARSG	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 1167186	NM_001267727.2(ARSG):c.903A>G (p.Gly301=)	ARSG	Single nucleotide variant (synonymous variant)	ARSG-related condition +1 more	GBenign
Select item 1356834	NM_001267727.2(ARSG):c.1004C>T (p.Thr335Met)	ARSG (T319M +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 782609	NM_001267727.2(ARSG):c.1092-5C>T	ARSG	Single nucleotide variant (intron variant)	ARSG-related condition +2 more	GBenign/Likely benign
Select item 1435253	NM_001267727.2(ARSG):c.1092C>T (p.Ser364=)	ARSG	Single nucleotide variant (synonymous variant)	ARSG-related condition +1 more	GConflicting classifications of pathogenicity
Select item 1111180	NM_001267727.2(ARSG):c.1113T>C (p.Thr371=)	ARSG	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1165739	NM_001267727.2(ARSG):c.1233C>T (p.Ser411=)	ARSG	Single nucleotide variant (synonymous variant)	ARSG-related condition +1 more	GBenign
Select item 2173474	NM_001267727.2(ARSG):c.1440C>G (p.Pro480=)	ARSG, PRKAR1A	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign
Select item 731552	NM_001267727.2(ARSG):c.1478T>C (p.Ile493Thr)	ARSG, PRKAR1A (I492T +1 more)	Single nucleotide variant (missense variant +1 more)	ARSG-related condition +1 more	GLikely benign
Select item 3048656	NM_001267727.2(ARSG):c.*10T>C	ARSG, PRKAR1A	Single nucleotide variant (3 prime UTR variant +1 more)	ARSG-related condition	GLikely benign
Select item 3047301	NM_017983.7(WIPI1):c.1152C>T (p.Thr384=)	ARSG, PRKAR1A +1 more	Single nucleotide variant (synonymous variant +2 more)	WIPI1-related disorder	GLikely benign
Select item 3045393	NM_017983.7(WIPI1):c.687G>A (p.Met229Ile)	ARSG, PRKAR1A +1 more (M147I +1 more)	Single nucleotide variant (missense variant +2 more)	WIPI1-related disorder	GLikely benign

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Items: 21