List of variants in gene SLC25A15 reported as likely pathogenic by Baylor 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: 21

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HGVS	dbSNP	gnomAD frequency
NM_014252.4(SLC25A15):c.815C>T (p.Thr272Ile)	rs121908535	0.00004
NM_014252.4(SLC25A15):c.538G>A (p.Glu180Lys)	rs104894424	0.00002
NM_014252.4(SLC25A15):c.824G>A (p.Arg275Gln)	rs104894431	0.00001
NM_014252.4(SLC25A15):c.169C>T (p.Gln57Ter)
NM_014252.4(SLC25A15):c.172del (p.Val58fs)
NM_014252.4(SLC25A15):c.212T>A (p.Leu71Gln)	rs121908534
NM_014252.4(SLC25A15):c.236C>G (p.Ser79Ter)	rs2138045987
NM_014252.4(SLC25A15):c.315-2A>C
NM_014252.4(SLC25A15):c.31_55del (p.Ile11fs)
NM_014252.4(SLC25A15):c.326del (p.Asn109fs)
NM_014252.4(SLC25A15):c.331_335del (p.Ala111fs)
NM_014252.4(SLC25A15):c.337G>T (p.Gly113Cys)	rs199894905
NM_014252.4(SLC25A15):c.357del (p.Phe119fs)
NM_014252.4(SLC25A15):c.408del (p.Met137fs)	rs780201405
NM_014252.4(SLC25A15):c.429_430del (p.Gly144fs)
NM_014252.4(SLC25A15):c.452+1del
NM_014252.4(SLC25A15):c.498del (p.Leu167fs)	rs2138056689
NM_014252.4(SLC25A15):c.514G>T (p.Gly172Ter)	rs1480063127
NM_014252.4(SLC25A15):c.530T>A (p.Leu177Ter)
NM_014252.4(SLC25A15):c.564C>G (p.Phe188Leu)	rs141028076
NM_014252.4(SLC25A15):c.622+1G>A	rs957788324

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