List of variants in gene SLC25A13 reported as benign by Invitae

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: 25

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HGVS	dbSNP	gnomAD frequency
NM_014251.3(SLC25A13):c.328+6A>G	rs6957975	0.67687
NM_014251.3(SLC25A13):c.1194A>G (p.Leu398=)	rs2301629	0.34968
NM_014251.3(SLC25A13):c.1884C>T (p.Asn628=)	rs35539807	0.02629
NM_014251.3(SLC25A13):c.1671C>T (p.Thr557=)	rs79886797	0.01284
NM_014251.3(SLC25A13):c.93T>C (p.Gly31=)	rs78430478	0.01089
NM_014251.3(SLC25A13):c.675G>A (p.Ser225=)	rs78247004	0.01022
NM_014251.3(SLC25A13):c.1374G>A (p.Val458=)	rs115266882	0.00605
NM_014251.3(SLC25A13):c.1680C>T (p.Ser560=)	rs150082469	0.00244
NM_014251.3(SLC25A13):c.1434G>T (p.Gly478=)	rs146111714	0.00178
NM_014251.3(SLC25A13):c.329-17G>C	rs185938432	0.00105
NM_014251.3(SLC25A13):c.1230+11T>C	rs201352939	0.00060
NM_014251.3(SLC25A13):c.1088G>T (p.Gly363Val)	rs35996658	0.00028
NM_014251.3(SLC25A13):c.1354G>A (p.Val452Ile)	rs143877538	0.00019
NM_014251.3(SLC25A13):c.1842-12C>A	rs201468457	0.00008
NM_014251.3(SLC25A13):c.576C>G (p.Pro192=)	rs753114158	0.00001
NM_014251.3(SLC25A13):c.1177+17C>G
NM_014251.3(SLC25A13):c.1312-12del	rs771217878
NM_014251.3(SLC25A13):c.1751-5del	rs1173610818
NM_014251.3(SLC25A13):c.212+14del
NM_014251.3(SLC25A13):c.213-10dup	rs752612661
NM_014251.3(SLC25A13):c.306T>C (p.Ala102=)	rs565008080
NM_014251.3(SLC25A13):c.329-4dup	rs1472181392
NM_014251.3(SLC25A13):c.70-14dup	rs751240780
NM_014251.3(SLC25A13):c.70-7del	rs751240780
NM_014251.3(SLC25A13):c.848+9G>T	rs201395793

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