ClinVar Miner

List of variants in gene SPINK5 reported as benign for not specified

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 64
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HGVS dbSNP gnomAD frequency
NM_006846.4(SPINK5):c.2313+48G>A rs9325074 0.79044
NM_006846.4(SPINK5):c.2667-13A>T rs2052537 0.78792
NM_006846.4(SPINK5):c.82-31A>G rs1423001 0.74351
NM_006846.4(SPINK5):c.209+72C>A rs3752676 0.70739
NM_006846.4(SPINK5):c.1888-54G>A rs3815735 0.69656
NM_006846.4(SPINK5):c.81+54G>A rs9325061 0.69401
NM_006846.4(SPINK5):c.81+88C>G rs1609851 0.69397
NM_006846.4(SPINK5):c.1659C>T (p.Val553=) rs2303071 0.58781
NM_006846.4(SPINK5):c.2965-46T>C rs6895434 0.56266
NM_006846.4(SPINK5):c.3009T>C (p.Gly1003=) rs2400478 0.56263
NM_006846.4(SPINK5):c.2740-59G>A rs2112767 0.56261
NM_006846.4(SPINK5):c.2241-26T>C rs3764926 0.56233
NM_006846.4(SPINK5):c.2132G>A (p.Arg711Gln) rs3777134 0.54171
NM_006846.4(SPINK5):c.2412C>T (p.Gly804=) rs33920397 0.54161
NM_006846.4(SPINK5):c.2358C>T (p.Leu786=) rs17704908 0.54150
NM_006846.4(SPINK5):c.2113-68T>C rs3777135 0.54145
NM_006846.4(SPINK5):c.2313+51G>A rs12518996 0.54077
NM_006846.4(SPINK5):c.882+45_882+46insT rs76839946 0.51324
NM_006846.4(SPINK5):c.2740-170G>A rs3764930 0.50854
NM_006846.4(SPINK5):c.800A>G (p.Gln267Arg) rs6892205 0.50665
NM_006846.4(SPINK5):c.474+66C>G rs7711953 0.46092
NM_006846.4(SPINK5):c.882+20A>G rs11958432 0.45982
NM_006846.4(SPINK5):c.1004C>T (p.Ala335Val) rs34482796 0.45563
NM_006846.4(SPINK5):c.1011-12C>T rs1422991 0.45033
NM_006846.4(SPINK5):c.1092+103C>A rs11168021 0.44349
NM_006846.4(SPINK5):c.1389A>G (p.Gly463=) rs6896303 0.44173
NM_006846.4(SPINK5):c.1302+19G>A rs2303068 0.44163
NM_006846.4(SPINK5):c.1221-50G>A rs2303066 0.44154
NM_006846.4(SPINK5):c.1258A>G (p.Lys420Glu) rs2303067 0.44148
NM_006846.4(SPINK5):c.1188T>C (p.His396=) rs2303065 0.44136
NM_006846.4(SPINK5):c.1093-26C>T rs2303061 0.44132
NM_006846.4(SPINK5):c.1103G>A (p.Ser368Asn) rs2303063 0.44127
NM_006846.4(SPINK5):c.*44T>C rs4349706 0.43753
NM_006846.4(SPINK5):c.1156G>A (p.Asp386Asn) rs2303064 0.24722
NM_006846.4(SPINK5):c.1820+74T>C rs2287768 0.16402
NM_006846.4(SPINK5):c.2475G>T (p.Glu825Asp) rs2303070 0.10250
NM_006846.4(SPINK5):c.1344G>A (p.Arg448=) rs17107741 0.05403
NM_006846.4(SPINK5):c.209+15C>T rs3752677 0.04511
NM_006846.4(SPINK5):c.2661C>G (p.Ser887Arg) rs28408445 0.04324
NM_006846.4(SPINK5):c.1431-75C>G rs10477362 0.04317
NM_006846.4(SPINK5):c.2965-10G>C rs58888156 0.04288
NM_006846.4(SPINK5):c.1851T>C (p.Ala617=) rs17718737 0.03431
NM_006846.4(SPINK5):c.316G>A (p.Asp106Asn) rs17860502 0.03121
NM_006846.4(SPINK5):c.531G>A (p.Arg177=) rs35121983 0.02736
NM_006846.4(SPINK5):c.2915A>G (p.His972Arg) rs17705005 0.02442
NM_006846.4(SPINK5):c.1552C>T (p.Arg518Cys) rs115504632 0.01067
NM_006846.4(SPINK5):c.1764T>G (p.Ile588Met) rs35877540 0.01015
NM_006846.4(SPINK5):c.2905A>G (p.Lys969Glu) rs3188691 0.00856
NM_006846.4(SPINK5):c.2241-6C>T rs190365795 0.00842
NM_006846.4(SPINK5):c.2667-4G>A rs180955184 0.00542
NM_006846.4(SPINK5):c.1093-10A>G rs2303062
NM_006846.4(SPINK5):c.1431-39del rs34473560
NM_006846.4(SPINK5):c.1557C>A (p.Gly519=) rs880687
NM_006846.4(SPINK5):c.1607+47C>T rs41291431
NM_006846.4(SPINK5):c.1607+93_1607+94del rs3036740
NM_006846.4(SPINK5):c.2313+31C>G rs9325073
NM_006846.4(SPINK5):c.2667-12del rs368593462
NM_006846.4(SPINK5):c.2667-13delinsTT rs1554106953
NM_006846.4(SPINK5):c.2667-14dup rs3036731
NM_006846.4(SPINK5):c.2667-15_2667-14dup rs3036731
NM_006846.4(SPINK5):c.3187-76C>T
NM_006846.4(SPINK5):c.475-443A>G
NM_006846.4(SPINK5):c.475-86G>C rs4529181
NM_006846.4(SPINK5):c.883-76_883-75insAATTT rs55959555

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