Related gene-specific medical variations for Gene (Select 54972) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3326753	NM_178031.3(TMEM132A):c.2278G>A (p.Gly760Ser)	LOC130005787, TMEM132A (G760S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3178688	NM_178031.3(TMEM132A):c.61C>G (p.Leu21Val)	LOC130005784, TMEM132A (L21V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3178675	NM_178031.3(TMEM132A):c.2299C>T (p.Pro767Ser)	LOC130005787, TMEM132A (P767S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3178674	NM_178031.3(TMEM132A):c.22C>G (p.Arg8Gly)	LOC130005784, TMEM132A (R8G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2592091	NM_178031.3(TMEM132A):c.2255G>A (p.Arg752His)	LOC130005787, TMEM132A (R752H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2394590	NM_178031.3(TMEM132A):c.2332T>A (p.Ser778Thr)	LOC130005787, TMEM132A (S778T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 780976	NM_178031.3(TMEM132A):c.2235C>A (p.Pro745=)	LOC130005787, TMEM132A	Single nucleotide variant (synonymous variant)	not provided	GBenign

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