"PreventionGenetics, part of Exact Sciences"[submitter] AND "STT3B"[ge - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3049939	NM_178862.3(STT3B):c.-7G>C	LOC129936407, STT3B	Single nucleotide variant (5 prime UTR variant)	STT3B-related disorder	GLikely benign
Select item 380194	NM_178862.3(STT3B):c.777+7T>G	STT3B	Single nucleotide variant (intron variant)	STT3B-related disorder +2 more	GBenign
Select item 389417	NM_178862.3(STT3B):c.2322A>G (p.Ala774=)	STT3B	Single nucleotide variant (synonymous variant)	STT3B-related disorder +2 more	GBenign/Likely benign

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