ClinVar Miner

Variants in gene NIN with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status: Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status: Submission 2 (benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 26
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HGVS dbSNP gnomAD frequency
NM_020921.4(NIN):c.933G>C (p.Leu311=) rs8020503 0.99252
NM_020921.4(NIN):c.5628+5T>C rs3015485 0.99236
NM_020921.4(NIN):c.5637G>A (p.Gln1879=) rs11376 0.56301
NM_020921.4(NIN):c.1128T>C (p.Val376=) rs17793018 0.52775
NM_020921.4(NIN):c.2616C>A (p.Ala872=) rs2073349 0.35221
NM_020921.4(NIN):c.3090A>T (p.Ser1030=) rs2073348 0.28854
NM_020921.4(NIN):c.3331C>G (p.Pro1111Ala) rs2236316 0.20068
NM_020921.4(NIN):c.5800C>G (p.Gln1934Glu) rs2295847 0.10087
NM_020921.4(NIN):c.5509T>A (p.Ser1837Thr) rs12717411 0.02104
NM_020921.4(NIN):c.3459G>A (p.Arg1153=) rs41310342 0.01853
NM_020921.4(NIN):c.819C>T (p.Phe273=) rs61755581 0.01567
NM_020921.4(NIN):c.1728G>A (p.Pro576=) rs61755036 0.01477
NM_020921.4(NIN):c.2651A>G (p.Lys884Arg) rs41299191 0.01436
NM_020921.4(NIN):c.4866A>C (p.Glu1622Asp) rs77959782 0.01304
NM_020921.4(NIN):c.600T>C (p.Gly200=) rs61740039 0.00982
NM_020921.4(NIN):c.3454G>T (p.Val1152Phe) rs61742284 0.00858
NM_020921.4(NIN):c.4674G>A (p.Thr1558=) rs45578537 0.00828
NM_020921.4(NIN):c.264A>T (p.Pro88=) rs61755037 0.00815
NM_020921.4(NIN):c.5903C>T (p.Thr1968Met) rs61744312 0.00758
NM_020921.4(NIN):c.6068A>G (p.Asn2023Ser) rs61747997 0.00620
NM_020921.4(NIN):c.4837C>T (p.Arg1613Cys) rs61755995 0.00434
NM_020921.4(NIN):c.612G>A (p.Arg204=) rs150057118 0.00118
NM_020921.4(NIN):c.4937G>A (p.Arg1646His) rs149669464 0.00096
NM_020921.4(NIN):c.399G>A (p.Ala133=) rs372665883 0.00011
NM_020921.4(NIN):c.1558G>C (p.Asp520His)
NM_020921.4(NIN):c.5912C>A (p.Pro1971Gln) rs200441923

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