List of variants in gene SLC25A22 reported as uncertain significance by Ambry Genetics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 34

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HGVS	dbSNP	gnomAD frequency
NM_001191061.2(SLC25A22):c.140C>T (p.Thr47Met)	rs142220309	0.00068
NM_001191061.2(SLC25A22):c.267C>G (p.Phe89Leu)	rs143064022	0.00024
NM_001191061.2(SLC25A22):c.679G>A (p.Val227Met)	rs200603610	0.00024
NM_001191061.2(SLC25A22):c.464G>C (p.Gly155Ala)	rs200992080	0.00016
NM_001191061.2(SLC25A22):c.653C>T (p.Ala218Val)	rs150645806	0.00014
NM_001191061.2(SLC25A22):c.647G>A (p.Arg216His)	rs201932343	0.00012
NM_001191061.2(SLC25A22):c.506C>T (p.Thr169Met)	rs533726078	0.00011
NM_001191061.2(SLC25A22):c.146+6T>C	rs369906148	0.00008
NM_001191061.2(SLC25A22):c.124G>A (p.Gly42Ser)	rs535927522	0.00007
NM_001191061.2(SLC25A22):c.46G>A (p.Gly16Ser)	rs149569043	0.00006
NM_001191061.2(SLC25A22):c.493G>A (p.Ala165Thr)	rs763227728	0.00005
NM_001191061.2(SLC25A22):c.*4C>G	rs1396699166	0.00004
NM_001191061.2(SLC25A22):c.562A>G (p.Lys188Glu)	rs767949941	0.00004
NM_001191061.2(SLC25A22):c.650C>T (p.Pro217Leu)	rs139555989	0.00004
NM_001191061.2(SLC25A22):c.190G>A (p.Gly64Ser)	rs774766308	0.00003
NM_001191061.2(SLC25A22):c.725C>T (p.Ala242Val)	rs781424186	0.00003
NM_001191061.2(SLC25A22):c.871C>T (p.Arg291Cys)	rs762897089	0.00003
NM_001191061.2(SLC25A22):c.494C>T (p.Ala165Val)	rs752791901	0.00002
NM_001191061.2(SLC25A22):c.535C>T (p.Arg179Trp)	rs574361397	0.00002
NM_001191061.2(SLC25A22):c.16A>G (p.Ile6Val)	rs1362967882	0.00001
NM_001191061.2(SLC25A22):c.467C>A (p.Ala156Asp)	rs1353048193	0.00001
NM_001191061.2(SLC25A22):c.829C>T (p.Arg277Trp)	rs567628237	0.00001
NM_001191061.2(SLC25A22):c.-5G>C
NM_001191061.2(SLC25A22):c.123C>G (p.Asn41Lys)
NM_001191061.2(SLC25A22):c.200G>A (p.Arg67Gln)
NM_001191061.2(SLC25A22):c.221C>T (p.Thr74Ile)
NM_001191061.2(SLC25A22):c.263A>G (p.Asp88Gly)	rs2133706338
NM_001191061.2(SLC25A22):c.316G>A (p.Glu106Lys)
NM_001191061.2(SLC25A22):c.344C>T (p.Thr115Ile)	rs1565037117
NM_001191061.2(SLC25A22):c.365C>T (p.Thr122Met)	rs778373047
NM_001191061.2(SLC25A22):c.524G>T (p.Arg175Leu)	rs769329043
NM_001191061.2(SLC25A22):c.784G>A (p.Glu262Lys)
NM_001191061.2(SLC25A22):c.887C>T (p.Ala296Val)	rs1565034826
NM_001191061.2(SLC25A22):c.938C>T (p.Ser313Phe)

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