ClinVar Miner

List of variants in gene ANKS6 studied for abdominal and pelvic region disorder

Included ClinVar conditions (956):
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Gene type:
ClinVar version:
Total variants: 32
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HGVS dbSNP
NM_173551.5(ANKS6):c.1007C>T (p.Thr336Met) rs376870807
NM_173551.5(ANKS6):c.1115A>G (p.Asn372Ser) rs201297615
NM_173551.5(ANKS6):c.1176T>G (p.Asn392Lys) rs776931798
NM_173551.5(ANKS6):c.1220-6C>T
NM_173551.5(ANKS6):c.1322A>G (p.Gln441Arg) rs377750405
NM_173551.5(ANKS6):c.1381C>T (p.Arg461Ter) rs369437168
NM_173551.5(ANKS6):c.1731G>A (p.Thr577=) rs201821907
NM_173551.5(ANKS6):c.1902G>A (p.Ser634=) rs765475331
NM_173551.5(ANKS6):c.1913C>T (p.Ser638Leu) rs200373053
NM_173551.5(ANKS6):c.1973-3C>G rs397514257
NM_173551.5(ANKS6):c.2052C>A (p.Ser684Arg) rs1554742278
NM_173551.5(ANKS6):c.2054_2064del (p.His685fs) rs587777024
NM_173551.5(ANKS6):c.2105C>T (p.Pro702Leu) rs760387934
NM_173551.5(ANKS6):c.2113C>T (p.Pro705Ser) rs146038901
NM_173551.5(ANKS6):c.2197A>C (p.Thr733Pro) rs201419783
NM_173551.5(ANKS6):c.2233G>A (p.Gly745Arg) rs202244716
NM_173551.5(ANKS6):c.2264C>T (p.Ser755Leu) rs370230003
NM_173551.5(ANKS6):c.2267C>T (p.Ser756Leu)
NM_173551.5(ANKS6):c.2327A>G (p.Asp776Gly) rs372265310
NM_173551.5(ANKS6):c.2370_2372del (p.Tyr790_Gln791delinsTer) rs587777025
NM_173551.5(ANKS6):c.238A>G (p.Thr80Ala) rs1554752436
NM_173551.5(ANKS6):c.2503G>A (p.Ala835Thr)
NM_173551.5(ANKS6):c.2512-2A>C rs397514258
NM_173551.5(ANKS6):c.413A>G (p.Asn138Ser) rs374511363
NM_173551.5(ANKS6):c.424C>T (p.Arg142Trp)
NM_173551.5(ANKS6):c.532G>A (p.Glu178Lys) rs181546859
NM_173551.5(ANKS6):c.539_540del (p.Leu180fs)
NM_173551.5(ANKS6):c.664C>G (p.Arg222Gly)
NM_173551.5(ANKS6):c.694_718dup (p.Val240fs) rs1564228101
NM_173551.5(ANKS6):c.727C>T (p.Gln243Ter) rs756090222
NM_173551.5(ANKS6):c.806A>G (p.Lys269Arg) rs200902480
NM_173551.5(ANKS6):c.847G>A (p.Val283Ile) rs748439897

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