List of variants in gene TMEM231 reported by CeGaT Center for Human Genetics Tuebingen

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: 16

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HGVS	dbSNP	gnomAD frequency
NM_001077418.3(TMEM231):c.928T>G (p.Leu310Val)	rs182008317	0.00181
NM_001077418.3(TMEM231):c.927C>A (p.Asp309Glu)	rs186119649	0.00179
NM_001077418.3(TMEM231):c.710G>C (p.Arg237Thr)	rs199813223	0.00141
NM_001077418.3(TMEM231):c.719A>G (p.Asp240Gly)	rs146210288	0.00138
NM_001077418.3(TMEM231):c.95C>T (p.Ala32Val)	rs201181950	0.00105
NM_001077418.3(TMEM231):c.-15C>T	rs138060715	0.00092
NM_001077418.3(TMEM231):c.139+42G>A	rs375718217	0.00024
NM_001077418.3(TMEM231):c.582C>T (p.Asn194=)	rs199776253	0.00024
NM_001077418.3(TMEM231):c.373C>G (p.Pro125Ala)	rs1442638461	0.00009
NM_001077418.3(TMEM231):c.45C>T (p.Tyr15=)	rs375077045	0.00009
NM_001077418.3(TMEM231):c.624C>T (p.Tyr208=)	rs368594302	0.00007
NM_001077418.3(TMEM231):c.582+6A>G	rs376300743	0.00006
NM_001077418.3(TMEM231):c.458T>A (p.Met153Lys)	rs2080678621
NM_001077418.3(TMEM231):c.648C>G (p.Ala216=)
NM_001077418.3(TMEM231):c.661A>T (p.Asn221Tyr)
NM_001077418.3(TMEM231):c.909A>C (p.Thr303=)

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