ClinVar Miner

List of variants in gene TTR reported as likely benign for ATTRV122I amyloidosis

Included ClinVar conditions (4):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 13
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HGVS dbSNP
NC_000018.10:g.31598936C>T
NM_000371.3(TTR):c.141T>C (p.Asn47=) rs1252826226
NM_000371.3(TTR):c.267C>T (p.Tyr89=) rs757950308
NM_000371.3(TTR):c.336+19G>A rs75517067
NM_000371.3(TTR):c.336+8T>C rs1176464590
NM_000371.3(TTR):c.355G>A (p.Asp119Asn) rs76410435
NM_000371.3(TTR):c.384C>T (p.Ala128=) rs143906738
NM_000371.3(TTR):c.405C>G (p.Ser135=) rs760153126
NM_000371.3(TTR):c.437A>G (p.Lys146Arg) rs536294863
NM_000371.4(TTR):c.195C>T (p.Ala65=) rs571695233
NM_000371.4(TTR):c.354C>T (p.Asn118=) rs11541797
NM_000371.4(TTR):c.416C>T (p.Thr139Met) rs28933981
NM_000371.4(TTR):c.69+10T>C rs1179187406

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