"PreventionGenetics, part of Exact Sciences"[submitter] AND "TMEM132E" - ClinVar - NCBI

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Items: 19

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1382833	NM_001304438.2(TMEM132E):c.111G>T (p.Pro37=)	TMEM132E	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 3048060	NM_001304438.2(TMEM132E):c.204C>A (p.Val68=)	TMEM132E	Single nucleotide variant (synonymous variant)	TMEM132E-related disorder	GLikely benign
Select item 3049673	NM_001304438.2(TMEM132E):c.330G>T (p.Pro110=)	TMEM132E	Single nucleotide variant (synonymous variant)	TMEM132E-related disorder	GLikely benign
Select item 1644183	NM_001304438.2(TMEM132E):c.470G>C (p.Gly157Ala)	TMEM132E (G157A)	Single nucleotide variant (missense variant)	TMEM132E-related disorder +1 more	GLikely benign
Select item 3053938	NM_001304438.2(TMEM132E):c.717T>C (p.Pro239=)	TMEM132E	Single nucleotide variant (synonymous variant)	TMEM132E-related disorder	GLikely benign
Select item 3044734	NM_001304438.2(TMEM132E):c.759G>A (p.Gly253=)	TMEM132E	Single nucleotide variant (synonymous variant)	TMEM132E-related disorder	GLikely benign
Select item 3037008	NM_001304438.2(TMEM132E):c.868C>T (p.Leu290=)	TMEM132E	Single nucleotide variant (synonymous variant)	TMEM132E-related disorder	GLikely benign
Select item 805612	NM_001304438.2(TMEM132E):c.915C>T (p.Pro305=)	TMEM132E	Single nucleotide variant (synonymous variant)	TMEM132E-related disorder +1 more	GBenign/Likely benign
Select item 1664370	NM_001304438.2(TMEM132E):c.962C>T (p.Ser321Leu)	TMEM132E (S321L)	Single nucleotide variant (missense variant)	TMEM132E-related disorder +1 more	GLikely benign
Select item 3052959	NM_001304438.2(TMEM132E):c.1145+8C>T	TMEM132E	Single nucleotide variant (intron variant)	TMEM132E-related disorder	GLikely benign
Select item 3035726	NM_001304438.2(TMEM132E):c.1242C>T (p.Asp414=)	TMEM132E	Single nucleotide variant (synonymous variant)	TMEM132E-related disorder	GLikely benign
Select item 1566575	NM_001304438.2(TMEM132E):c.1290G>A (p.Glu430=)	TMEM132E	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 2716884	NM_001304438.2(TMEM132E):c.1296G>A (p.Thr432=)	TMEM132E	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 143842	NM_001304438.2(TMEM132E):c.1529G>A (p.Arg510Gln)	TMEM132E (R510Q)	Single nucleotide variant (missense variant)	TMEM132E-related disorder	GUncertain significance
Select item 805610	NM_001304438.2(TMEM132E):c.2025G>A (p.Thr675=)	TMEM132E	Single nucleotide variant (synonymous variant)	TMEM132E-related disorder +1 more	GBenign
Select item 501073	NM_001304438.2(TMEM132E):c.2300G>A (p.Arg767Gln)	TMEM132E (R767Q)	Single nucleotide variant (missense variant)	not specified +2 more	GLikely benign
Select item 1656574	NM_001304438.2(TMEM132E):c.2445G>A (p.Arg815=)	TMEM132E	Single nucleotide variant (synonymous variant)	TMEM132E-related disorder +1 more	GLikely benign
Select item 1531603	NM_001304438.2(TMEM132E):c.2617C>T (p.Leu873=)	TMEM132E	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 1539694	NM_001304438.2(TMEM132E):c.2943C>T (p.Ser981=)	TMEM132E	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign