ClinVar Miner

List of variants in gene SERPINH1 reported as likely benign for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 98
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001235.5(SERPINH1):c.955-6C>A rs7105575 0.03189
NM_001235.5(SERPINH1):c.622+228C>T rs115945601 0.00880
NM_001235.5(SERPINH1):c.-34-103G>A rs147548875 0.00692
NM_001235.5(SERPINH1):c.622+223G>C rs148644113 0.00674
NM_001235.5(SERPINH1):c.622+257A>G rs142147918 0.00551
NM_001235.5(SERPINH1):c.-34-99C>T rs76649778 0.00382
NM_001235.5(SERPINH1):c.744C>T (p.Asp248=) rs61733248 0.00285
NM_001235.5(SERPINH1):c.722-13G>A rs116506210 0.00185
NM_001235.5(SERPINH1):c.721+9T>C rs138193444 0.00158
NM_001235.5(SERPINH1):c.267G>A (p.Thr89=) rs139127426 0.00155
NM_001235.5(SERPINH1):c.1219G>C (p.Val407Leu) rs138241050 0.00133
NM_001235.5(SERPINH1):c.580C>A (p.Arg194Ser) rs141721173 0.00100
NM_001235.5(SERPINH1):c.92G>C (p.Gly31Ala) rs140588417 0.00089
NM_001235.5(SERPINH1):c.492C>T (p.Arg164=) rs150586616 0.00078
NM_001235.5(SERPINH1):c.915C>T (p.Ser305=) rs147740415 0.00057
NM_001235.5(SERPINH1):c.97G>C (p.Ala33Pro) rs150061926 0.00043
NM_001235.5(SERPINH1):c.188C>T (p.Ala63Val) rs576480194 0.00038
NM_001235.5(SERPINH1):c.481A>C (p.Ile161Leu) rs112083274 0.00027
NM_001235.5(SERPINH1):c.1119C>T (p.Arg373=) rs375913094 0.00026
NM_001235.5(SERPINH1):c.293G>A (p.Ser98Asn) rs541595707 0.00023
NM_001235.5(SERPINH1):c.840C>T (p.Arg280=) rs149585133 0.00012
NM_001235.5(SERPINH1):c.1059C>T (p.His353=) rs199548932 0.00011
NM_001235.5(SERPINH1):c.298G>A (p.Glu100Lys) rs749665611 0.00011
NM_001235.5(SERPINH1):c.1113C>T (p.Tyr371=) rs533870576 0.00008
NM_001235.5(SERPINH1):c.168G>A (p.Gln56=) rs754091752 0.00007
NM_001235.5(SERPINH1):c.1149C>T (p.Tyr383=) rs201843800 0.00006
NM_001235.5(SERPINH1):c.1152C>T (p.Ala384=) rs368586977 0.00006
NM_001235.5(SERPINH1):c.102G>A (p.Glu34=) rs555812743 0.00005
NM_001235.5(SERPINH1):c.600A>C (p.Leu200=) rs764723506 0.00004
NM_001235.5(SERPINH1):c.565A>G (p.Thr189Ala) rs138784081 0.00003
NM_001235.5(SERPINH1):c.690T>C (p.Tyr230=) rs951634715 0.00003
NM_001235.5(SERPINH1):c.1191C>T (p.Ser397=) rs371506866 0.00002
NM_001235.5(SERPINH1):c.167A>G (p.Gln56Arg) rs553519612 0.00002
NM_001235.5(SERPINH1):c.622+7C>T rs757033716 0.00002
NM_001235.5(SERPINH1):c.160T>C (p.Leu54=) rs540061657 0.00001
NM_001235.5(SERPINH1):c.393C>T (p.Gly131=) rs760571465 0.00001
NM_001235.5(SERPINH1):c.741C>T (p.Asp247=) rs149910134 0.00001
NM_001235.5(SERPINH1):c.78C>T (p.Ala26=) rs763412073 0.00001
NM_001235.5(SERPINH1):c.831T>C (p.Pro277=) rs373407071 0.00001
NM_001235.5(SERPINH1):c.843T>C (p.Leu281=) rs544719966 0.00001
NM_001235.5(SERPINH1):c.861A>G (p.Lys287=) rs748644655 0.00001
NM_001235.5(SERPINH1):c.108G>A (p.Leu36=)
NM_001235.5(SERPINH1):c.1092C>T (p.Asn364=)
NM_001235.5(SERPINH1):c.1101C>T (p.Asp367=)
NM_001235.5(SERPINH1):c.1110C>A (p.Ile370=)
NM_001235.5(SERPINH1):c.1173A>G (p.Leu391=)
NM_001235.5(SERPINH1):c.1176G>A (p.Val392=)
NM_001235.5(SERPINH1):c.1185C>T (p.Thr395=)
NM_001235.5(SERPINH1):c.1212G>T (p.Gly404=) rs751357085
NM_001235.5(SERPINH1):c.1227T>C (p.Pro409=)
NM_001235.5(SERPINH1):c.1248C>T (p.Asp416=)
NM_001235.5(SERPINH1):c.150G>A (p.Leu50=) rs1592200249
NM_001235.5(SERPINH1):c.227C>T (p.Ser76Leu)
NM_001235.5(SERPINH1):c.240C>T (p.Leu80=)
NM_001235.5(SERPINH1):c.246G>A (p.Ser82=) rs930740979
NM_001235.5(SERPINH1):c.27C>T (p.Ala9=) rs1592199909
NM_001235.5(SERPINH1):c.30C>T (p.Phe10=)
NM_001235.5(SERPINH1):c.312C>T (p.Asp104=)
NM_001235.5(SERPINH1):c.333G>A (p.Leu111=)
NM_001235.5(SERPINH1):c.346C>A (p.Arg116Ser) rs200265134
NM_001235.5(SERPINH1):c.357C>T (p.Ser119=)
NM_001235.5(SERPINH1):c.426C>T (p.Phe142=)
NM_001235.5(SERPINH1):c.438C>T (p.Phe146=)
NM_001235.5(SERPINH1):c.444C>T (p.Arg148=)
NM_001235.5(SERPINH1):c.477C>T (p.Ser159=)
NM_001235.5(SERPINH1):c.504C>T (p.Ser168=)
NM_001235.5(SERPINH1):c.516C>T (p.Ser172=) rs1942095661
NM_001235.5(SERPINH1):c.51G>C (p.Leu17=) rs1320836204
NM_001235.5(SERPINH1):c.522C>T (p.Asn174=)
NM_001235.5(SERPINH1):c.534G>A (p.Ala178=)
NM_001235.5(SERPINH1):c.543C>G (p.Thr181=)
NM_001235.5(SERPINH1):c.54C>T (p.Ala18=)
NM_001235.5(SERPINH1):c.558C>T (p.Pro186=)
NM_001235.5(SERPINH1):c.585G>A (p.Thr195=)
NM_001235.5(SERPINH1):c.595C>T (p.Leu199=)
NM_001235.5(SERPINH1):c.622+12G>A
NM_001235.5(SERPINH1):c.622+8G>A
NM_001235.5(SERPINH1):c.622+8G>T rs781004270
NM_001235.5(SERPINH1):c.623-20G>A
NM_001235.5(SERPINH1):c.63G>A (p.Val21=)
NM_001235.5(SERPINH1):c.714C>T (p.His238=) rs761932276
NM_001235.5(SERPINH1):c.722-12C>T rs774226247
NM_001235.5(SERPINH1):c.722-14C>T rs901403627
NM_001235.5(SERPINH1):c.722-15C>T
NM_001235.5(SERPINH1):c.722-7C>T
NM_001235.5(SERPINH1):c.732C>T (p.Asn244=)
NM_001235.5(SERPINH1):c.738C>T (p.Tyr246=)
NM_001235.5(SERPINH1):c.804C>T (p.Ile268=) rs1942150058
NM_001235.5(SERPINH1):c.819T>C (p.His273=)
NM_001235.5(SERPINH1):c.858C>G (p.Thr286=)
NM_001235.5(SERPINH1):c.87T>A (p.Ala29=)
NM_001235.5(SERPINH1):c.936G>A (p.Glu312=)
NM_001235.5(SERPINH1):c.93C>A (p.Gly31=)
NM_001235.5(SERPINH1):c.954+15_954+18dup
NM_001235.5(SERPINH1):c.955-10del
NM_001235.5(SERPINH1):c.955-19C>T
NM_001235.5(SERPINH1):c.955-7C>T
NM_001235.5(SERPINH1):c.969G>T (p.Gly323=)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.