ClinVar Miner

List of variants in gene AVPR2 reported as likely pathogenic for diabetes insipidus

Included ClinVar conditions (7):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 23
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HGVS dbSNP gnomAD frequency
NM_000054.7(AVPR2):c.604C>T (p.Arg202Cys) rs782806507 0.00001
NM_000054.7(AVPR2):c.963C>A (p.Asn321Lys) rs193922123 0.00001
NM_000054.7(AVPR2):c.176T>C (p.Leu59Pro) rs193922112
NM_000054.7(AVPR2):c.290T>C (p.Leu97Pro) rs193922113
NM_000054.7(AVPR2):c.310C>T (p.Arg104Cys) rs104894760
NM_000054.7(AVPR2):c.335G>T (p.Cys112Phe) rs1057518723
NM_000054.7(AVPR2):c.382_384del (p.Tyr128del) rs1557100594
NM_000054.7(AVPR2):c.383A>C (p.Tyr128Ser) rs781950164
NM_000054.7(AVPR2):c.409C>G (p.Arg137Gly) rs104894761
NM_000054.7(AVPR2):c.424del (p.Cys142fs) rs193922114
NM_000054.7(AVPR2):c.472del (p.Arg158fs) rs193922115
NM_000054.7(AVPR2):c.513C>G (p.Ser171Arg) rs782601647
NM_000054.7(AVPR2):c.522G>T (p.Gln174His)
NM_000054.7(AVPR2):c.554del (p.Gly185fs) rs193922116
NM_000054.7(AVPR2):c.673C>T (p.Gln225Ter) rs193922117
NM_000054.7(AVPR2):c.752_758del (p.Arg251fs) rs193922118
NM_000054.7(AVPR2):c.770del (p.Gly257fs) rs193922119
NM_000054.7(AVPR2):c.814A>G (p.Met272Val) rs2064966794
NM_000054.7(AVPR2):c.816G>A (p.Met272Ile) rs1603282342
NM_000054.7(AVPR2):c.819_821del (p.Leu274del) rs193922120
NM_000054.7(AVPR2):c.853G>C (p.Ala285Pro) rs193922122
NM_000054.7(AVPR2):c.964C>A (p.Pro322Thr) rs2148515160
NM_000054.7(AVPR2):c.993dup (p.Val332fs)

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