ClinVar Miner

List of variants in gene SAR1B reported as likely benign for not provided

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Gene type:
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Total variants: 75
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HGVS dbSNP gnomAD frequency
NM_016103.4(SAR1B):c.349-84T>G rs13187174 0.02152
NM_016103.4(SAR1B):c.58+149A>T rs145209918 0.00504
NM_016103.4(SAR1B):c.59-23C>A rs79192135 0.00474
NM_016103.4(SAR1B):c.59-51G>A rs111280103 0.00387
NM_016103.4(SAR1B):c.480+102T>C rs116366212 0.00377
NM_016103.4(SAR1B):c.481-13T>C rs147455014 0.00353
NM_016103.4(SAR1B):c.321G>A (p.Arg107=) rs140899111 0.00121
NM_016103.4(SAR1B):c.244+9C>G rs200681744 0.00019
NM_016103.4(SAR1B):c.204C>T (p.Gly68=) rs143243934 0.00005
NM_016103.4(SAR1B):c.210G>A (p.Thr70=) rs757812045 0.00004
NM_016103.4(SAR1B):c.183C>T (p.Ser61=) rs769067083 0.00003
NM_016103.4(SAR1B):c.255G>A (p.Val85=) rs768368190 0.00002
NM_016103.4(SAR1B):c.141T>C (p.Asp47=) rs1193075817 0.00001
NM_016103.4(SAR1B):c.195C>T (p.Thr65=) rs770392723 0.00001
NM_016103.4(SAR1B):c.244+10T>C rs746508358 0.00001
NM_016103.4(SAR1B):c.245-20C>G rs1043685169 0.00001
NM_016103.4(SAR1B):c.481-18G>T rs373250763 0.00001
NM_016103.4(SAR1B):c.495G>C (p.Leu165=) rs140728989 0.00001
NM_016103.4(SAR1B):c.502C>T (p.Leu168=) rs1175873618 0.00001
NM_016103.4(SAR1B):c.510C>T (p.Ala170=) rs759070201 0.00001
NM_016103.4(SAR1B):c.59-4G>T rs763796886 0.00001
NM_016103.4(SAR1B):c.121T>C (p.Leu41=)
NM_016103.4(SAR1B):c.178+12C>G
NM_016103.4(SAR1B):c.178+17A>G
NM_016103.4(SAR1B):c.179-10T>C
NM_016103.4(SAR1B):c.179-18T>C
NM_016103.4(SAR1B):c.179-5T>C
NM_016103.4(SAR1B):c.228G>C (p.Leu76=)
NM_016103.4(SAR1B):c.244+11T>A
NM_016103.4(SAR1B):c.244+17T>A
NM_016103.4(SAR1B):c.244+18T>C rs1765236650
NM_016103.4(SAR1B):c.244+20_244+49del
NM_016103.4(SAR1B):c.244+9C>A rs200681744
NM_016103.4(SAR1B):c.244+9C>T rs200681744
NM_016103.4(SAR1B):c.244+9_244+10dup
NM_016103.4(SAR1B):c.244+9_244+11del rs1399435243
NM_016103.4(SAR1B):c.244+9_244+14dup
NM_016103.4(SAR1B):c.244+9_244+15dup rs762490675
NM_016103.4(SAR1B):c.244+9_244+16del
NM_016103.4(SAR1B):c.244+9_244+17dup
NM_016103.4(SAR1B):c.244+9_244+19del rs1477618348
NM_016103.4(SAR1B):c.244+9_244+23del
NM_016103.4(SAR1B):c.244+9_244+26del
NM_016103.4(SAR1B):c.244+9del
NM_016103.4(SAR1B):c.245-7T>C
NM_016103.4(SAR1B):c.246T>G (p.Ala82=)
NM_016103.4(SAR1B):c.276T>C (p.Ala92=)
NM_016103.4(SAR1B):c.297G>A (p.Leu99=)
NM_016103.4(SAR1B):c.312C>T (p.Asp104=) rs780986874
NM_016103.4(SAR1B):c.318A>G (p.Glu106=)
NM_016103.4(SAR1B):c.327A>G (p.Leu109=)
NM_016103.4(SAR1B):c.345T>C (p.Leu115=)
NM_016103.4(SAR1B):c.348+20C>T rs1765179851
NM_016103.4(SAR1B):c.349-11G>C
NM_016103.4(SAR1B):c.349-11_349-9del
NM_016103.4(SAR1B):c.349-16G>C
NM_016103.4(SAR1B):c.36C>T (p.Phe12=)
NM_016103.4(SAR1B):c.378T>C (p.Asn126=)
NM_016103.4(SAR1B):c.423C>T (p.Ala141=)
NM_016103.4(SAR1B):c.426C>T (p.Ile142=) rs2150049689
NM_016103.4(SAR1B):c.432A>G (p.Glu144=)
NM_016103.4(SAR1B):c.444A>G (p.Arg148=)
NM_016103.4(SAR1B):c.480+11A>T
NM_016103.4(SAR1B):c.480+14_480+15insG rs2150049637
NM_016103.4(SAR1B):c.480+19T>A
NM_016103.4(SAR1B):c.481-7A>T
NM_016103.4(SAR1B):c.534T>C (p.Cys178=)
NM_016103.4(SAR1B):c.549A>G (p.Arg183=)
NM_016103.4(SAR1B):c.558C>T (p.Tyr186=)
NM_016103.4(SAR1B):c.58+9G>A
NM_016103.4(SAR1B):c.59-145G>A rs139196971
NM_016103.4(SAR1B):c.59-18A>G rs2150054218
NM_016103.4(SAR1B):c.59-19C>G
NM_016103.4(SAR1B):c.591T>C (p.Ile197=) rs2150049090
NM_016103.4(SAR1B):c.63A>G (p.Leu21=)

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