List of variants in gene RINT1 studied for liver 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: 12

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HGVS	dbSNP	gnomAD frequency
NM_021930.6(RINT1):c.118A>T (p.Ser40Cys)	rs11556986	0.19903
NM_021930.6(RINT1):c.388G>A (p.Ala130Thr)	rs138345617	0.00060
NM_021930.6(RINT1):c.840-12T>A	rs747803201	0.00006
NM_021930.6(RINT1):c.1333+1G>A	rs375350359	0.00005
NM_021930.6(RINT1):c.1102G>A (p.Ala368Thr)	rs545894353	0.00001
NM_021930.6(RINT1):c.1120C>T (p.Arg374Trp)	rs1269514574	0.00001
NM_021930.6(RINT1):c.1285C>A (p.Leu429Ile)	rs1790880304	0.00001
NM_021930.6(RINT1):c.1109T>C (p.Leu370Pro)	rs1562849964
NM_021930.6(RINT1):c.1333+1G>T	rs375350359
NM_021930.6(RINT1):c.1853_1858del (p.Val618_Lys619del)	rs1554367227
NM_021930.6(RINT1):c.29C>A (p.Ser10Tyr)	rs1301146115
NM_021930.6(RINT1):c.604C>T (p.Gln202Ter)	rs1562847240

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