"PreventionGenetics, part of Exact Sciences"[submitter] AND "TMEM132D- - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3034662	NM_133448.3(TMEM132D):c.1443+6T>C	TMEM132D, TMEM132D-AS2	Single nucleotide variant (intron variant)	TMEM132D-related disorder	GLikely benign
Select item 3040955	NM_133448.3(TMEM132D):c.1353G>A (p.Pro451=)	TMEM132D, TMEM132D-AS2	Single nucleotide variant (non-coding transcript variant +1 more)	TMEM132D-related disorder	GLikely benign