ClinVar Miner

Variants in gene WHRN with conflicting interpretations "likely benign" and "uncertain significance"

Submission 1 (likely benign) minimum review status: Submission 1 (likely benign) method:
Submission 2 (uncertain significance) minimum review status: Submission 2 (uncertain significance) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 23
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HGVS dbSNP
NM_015404.4(WHRN):c.1048C>T (p.Arg350Trp) rs142990800
NM_015404.4(WHRN):c.1126G>T (p.Ala376Ser) rs545251395
NM_015404.4(WHRN):c.1365T>C (p.Ser455=) rs111033459
NM_015404.4(WHRN):c.1417-8G>A rs202228471
NM_015404.4(WHRN):c.1455G>A (p.Pro485=) rs141807746
NM_015404.4(WHRN):c.1627-5T>A rs187221008
NM_015404.4(WHRN):c.1632T>C (p.Thr544=) rs759107735
NM_015404.4(WHRN):c.1678G>A (p.Ala560Thr) rs182072601
NM_015404.4(WHRN):c.1696G>C (p.Val566Leu) rs189654215
NM_015404.4(WHRN):c.191C>A (p.Ala64Asp) rs146655362
NM_015404.4(WHRN):c.1943C>A (p.Ser648Tyr) rs142653982
NM_015404.4(WHRN):c.19G>C (p.Gly7Arg) rs572671060
NM_015404.4(WHRN):c.2112G>T (p.Leu704=) rs535492772
NM_015404.4(WHRN):c.2193C>T (p.Ser731=) rs147358257
NM_015404.4(WHRN):c.2203G>A (p.Val735Ile) rs373552185
NM_015404.4(WHRN):c.2237-10C>G rs200131193
NM_015404.4(WHRN):c.2333G>A (p.Arg778Gln) rs727505188
NM_015404.4(WHRN):c.2438C>T (p.Thr813Met)
NM_015404.4(WHRN):c.2644C>A (p.Arg882Ser) rs150586098
NM_015404.4(WHRN):c.33C>G (p.Ser11Arg) rs45527543
NM_015404.4(WHRN):c.376G>A (p.Ala126Thr)
NM_015404.4(WHRN):c.995G>A (p.Arg332Gln) rs139193948
NM_015404.4(WHRN):c.998G>A (p.Ser333Asn) rs200073414

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