ClinVar Miner

List of variants in gene ARL6 studied for abdominal and pelvic region disorder

Included ClinVar conditions (1030):
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Gene type:
ClinVar version:
Total variants: 50
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HGVS dbSNP
GRCh38/hg38 3q11.2(chr3:97790061-97794169)
NC_000003.12:g.(?_97768108)_(97768230_?)del
NM_001278293.3(ARL6):c.*225G>C rs4857294
NM_001278293.3(ARL6):c.*255C>T rs79196822
NM_001278293.3(ARL6):c.*275G>A rs886058939
NM_001278293.3(ARL6):c.*284C>A rs148380165
NM_001278293.3(ARL6):c.*309T>C
NM_001278293.3(ARL6):c.*470G>A rs184213166
NM_001278293.3(ARL6):c.*495C>T
NM_001278293.3(ARL6):c.-137A>C rs192372191
NM_001278293.3(ARL6):c.-146T>C rs886058937
NM_001278293.3(ARL6):c.-207G>A rs189005414
NM_001278293.3(ARL6):c.-240C>T rs116162146
NM_001278293.3(ARL6):c.-27-1461A>T rs143739859
NM_001278293.3(ARL6):c.-71C>G rs777066573
NM_001278293.3(ARL6):c.121A>G (p.Asn41Asp)
NM_001278293.3(ARL6):c.140T>A (p.Ile47Asn) rs757995078
NM_001278293.3(ARL6):c.185+1G>C rs1559679965
NM_001278293.3(ARL6):c.192A>G (p.Ser64=) rs140114162
NM_001278293.3(ARL6):c.266C>A (p.Ala89Asp)
NM_001278293.3(ARL6):c.266C>G (p.Ala89Gly)
NM_001278293.3(ARL6):c.272T>C (p.Ile91Thr) rs137854907
NM_001278293.3(ARL6):c.291T>A (p.Ser97Arg)
NM_001278293.3(ARL6):c.306G>A (p.Met102Ile)
NM_001278293.3(ARL6):c.317A>G (p.Lys106Arg)
NM_001278293.3(ARL6):c.341A>G (p.Asn114Ser)
NM_001278293.3(ARL6):c.350-13_350-2del rs1576465252
NM_001278293.3(ARL6):c.350-7C>T rs375454860
NM_001278293.3(ARL6):c.351_353delinsGAAAA (p.Asp117fs) rs1057515576
NM_001278293.3(ARL6):c.364C>T (p.Arg122Ter) rs104893678
NM_001278293.3(ARL6):c.365G>A (p.Arg122Gln)
NM_001278293.3(ARL6):c.365G>C (p.Arg122Pro)
NM_001278293.3(ARL6):c.40_42AAG[2] (p.Lys16del)
NM_001278293.3(ARL6):c.442T>G (p.Cys148Gly) rs148745414
NM_001278293.3(ARL6):c.480-8C>T rs77010939
NM_001278293.3(ARL6):c.493A>G (p.Ile165Val)
NM_001278293.3(ARL6):c.499G>A (p.Gly167Arg)
NM_001278293.3(ARL6):c.506G>C (p.Gly169Ala) rs104893679
NM_001278293.3(ARL6):c.506del (p.Gly169fs)
NM_001278293.3(ARL6):c.509T>G (p.Leu170Trp) rs104893681
NM_001278293.3(ARL6):c.526T>C (p.Trp176Arg) rs886058938
NM_001278293.3(ARL6):c.528G>T (p.Trp176Cys)
NM_001278293.3(ARL6):c.535G>A (p.Asp179Asn)
NM_001278293.3(ARL6):c.536-4T>C rs201939836
NM_001278293.3(ARL6):c.550G>T (p.Val184Leu)
NM_001278293.3(ARL6):c.551_552del (p.Val184fs)
NM_001278293.3(ARL6):c.92C>G (p.Thr31Arg) rs104893680
NM_001278293.3(ARL6):c.92C>T (p.Thr31Met) rs104893680
NM_032146.5(ARL6):c.-411A>G
NM_032146.5(ARL6):c.-415C>T

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