"PreventionGenetics, part of Exact Sciences"[submitter] AND "SIN3B"[ge - ClinVar

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Items: 20

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3040879	NM_001297595.2(SIN3B):c.365C>T (p.Ser122Leu)	SIN3B (S122L)	Single nucleotide variant (missense variant)	SIN3B-related disorder	GLikely benign
Select item 3034782	NM_001297595.2(SIN3B):c.576G>A (p.Thr192=)	SIN3B	Single nucleotide variant (synonymous variant)	SIN3B-related disorder	GLikely benign
Select item 2637120	NM_001297595.2(SIN3B):c.731C>G (p.Thr244Arg)	SIN3B (T244R)	Single nucleotide variant (missense variant)	SIN3B-related disorder	GUncertain significance
Select item 3052153	NM_001297595.2(SIN3B):c.759C>T (p.Ser253=)	SIN3B	Single nucleotide variant (synonymous variant)	SIN3B-related disorder	GLikely benign
Select item 3044602	NM_001297595.2(SIN3B):c.1120G>A (p.Ala374Thr)	SIN3B (A374T)	Single nucleotide variant (missense variant)	SIN3B-related disorder	GLikely benign
Select item 709302	NM_001297595.2(SIN3B):c.1266+335G>A	SIN3B (W426*)	Single nucleotide variant (nonsense +1 more)	SIN3B-related disorder +1 more	GBenign/Likely benign
Select item 3049595	NM_001297595.2(SIN3B):c.1389C>T (p.Asp463=)	SIN3B	Single nucleotide variant (synonymous variant)	SIN3B-related disorder	GLikely benign
Select item 3055351	NM_001297595.2(SIN3B):c.1452T>C (p.Ser484=)	SIN3B	Single nucleotide variant (synonymous variant)	SIN3B-related disorder	GBenign
Select item 3040221	NM_001297595.2(SIN3B):c.1509G>A (p.Thr503=)	SIN3B	Single nucleotide variant (synonymous variant)	SIN3B-related disorder	GLikely benign
Select item 3040128	NM_001297595.2(SIN3B):c.1599C>T (p.Thr533=)	SIN3B	Single nucleotide variant (synonymous variant)	SIN3B-related disorder	GLikely benign
Select item 3036137	NM_001297595.2(SIN3B):c.1848C>T (p.Ser616=)	SIN3B	Single nucleotide variant (synonymous variant)	SIN3B-related disorder	GLikely benign
Select item 3042916	NM_001297595.2(SIN3B):c.2031C>T (p.Ser677=)	SIN3B	Single nucleotide variant (synonymous variant)	SIN3B-related disorder	GLikely benign
Select item 3034407	NM_001297595.2(SIN3B):c.2102C>T (p.Pro701Leu)	SIN3B (P291L +2 more)	Single nucleotide variant (missense variant)	SIN3B-related disorder	GLikely benign
Select item 3044305	NM_001297595.2(SIN3B):c.2184G>A (p.Pro728=)	SIN3B	Single nucleotide variant (synonymous variant)	SIN3B-related disorder	GLikely benign
Select item 3041466	NM_001297595.2(SIN3B):c.2204C>T (p.Pro735Leu)	SIN3B (P325L +2 more)	Single nucleotide variant (missense variant)	SIN3B-related disorder	GBenign
Select item 2631283	NM_001297595.2(SIN3B):c.2340G>T (p.Glu780Asp)	SIN3B (E370D +2 more)	Single nucleotide variant (missense variant)	SIN3B-related disorder	GUncertain significance
Select item 3053118	NM_001297595.2(SIN3B):c.2423-4G>A	SIN3B	Single nucleotide variant (intron variant)	SIN3B-related disorder	GLikely benign
Select item 3041154	NM_001297595.2(SIN3B):c.2523C>T (p.Arg841=)	SIN3B	Single nucleotide variant (synonymous variant)	SIN3B-related disorder	GLikely benign
Select item 1303542	NM_001297595.2(SIN3B):c.2954+6A>G	SIN3B	Single nucleotide variant (intron variant)	SIN3B-related disorder +1 more	GBenign
Select item 3042581	NM_001297595.2(SIN3B):c.2955-7C>T	SIN3B	Single nucleotide variant (intron variant)	SIN3B-related disorder	GLikely benign

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Items: 20