List of variants in gene SLC26A8 studied for spermatogenic failure

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_052961.4(SLC26A8):c.2434G>A (p.Glu812Lys)	rs142724470	0.00075
NM_052961.4(SLC26A8):c.260G>A (p.Arg87Gln)	rs140210148	0.00031
NM_052961.4(SLC26A8):c.2860C>T (p.Arg954Cys)	rs398123027	0.00003
NM_052961.4(SLC26A8):c.290T>C (p.Leu97Pro)	rs1220970427	0.00001
NM_052961.4(SLC26A8):c.1664del (p.Ile555fs)	rs2127298549
NM_052961.4(SLC26A8):c.2031T>G (p.Tyr677Ter)
NM_052961.4(SLC26A8):c.212G>T (p.Arg71Leu)	rs116146081

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