ClinVar Miner

List of variants in gene HERC2 reported as likely benign for not provided

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Gene type:
ClinVar version:
Total variants: 167
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HGVS dbSNP gnomAD frequency
NM_004667.6(HERC2):c.9885G>A (p.Thr3295=) rs113016718 0.01043
NM_004667.6(HERC2):c.4009C>T (p.Leu1337Phe) rs145594989 0.00991
NM_004667.6(HERC2):c.10274C>T (p.Pro3425Leu) rs147705404 0.00400
NM_004667.6(HERC2):c.643+5G>A rs117411594 0.00367
NM_004667.6(HERC2):c.6555+3G>A rs151156359 0.00302
NM_004667.6(HERC2):c.5577A>T (p.Ser1859=) rs200997244 0.00286
NM_004667.6(HERC2):c.5440A>G (p.Thr1814Ala) rs138650689 0.00266
NM_004667.6(HERC2):c.10969G>A (p.Val3657Ile) rs139953376 0.00265
NM_004667.6(HERC2):c.5429T>C (p.Met1810Thr) rs142072884 0.00260
NM_004667.6(HERC2):c.2389A>G (p.Met797Val) rs150930758 0.00206
NM_004667.6(HERC2):c.8187T>C (p.Phe2729=) rs146864624 0.00205
NM_004667.6(HERC2):c.3687C>T (p.Asp1229=) rs149204675 0.00190
NM_004667.6(HERC2):c.6558C>T (p.Ala2186=) rs559761830 0.00180
NM_004667.6(HERC2):c.7058C>G (p.Thr2353Ser) rs145370046 0.00155
NM_004667.6(HERC2):c.7316C>A (p.Ala2439Asp) rs200823016 0.00150
NM_004667.6(HERC2):c.5799T>A (p.Ala1933=) rs142034055 0.00132
NM_004667.6(HERC2):c.4318T>C (p.Leu1440=) rs2525981 0.00111
NM_004667.6(HERC2):c.9939C>T (p.Arg3313=) rs117437554 0.00096
NM_004667.6(HERC2):c.3357G>A (p.Ala1119=) rs140345440 0.00084
NM_004667.6(HERC2):c.3828G>A (p.Ala1276=) rs2525976 0.00081
NM_004667.6(HERC2):c.2747-3C>A rs200632307 0.00076
NM_004667.6(HERC2):c.6123C>T (p.Gly2041=) rs148503135 0.00076
NM_004667.6(HERC2):c.5391C>T (p.His1797=) rs200571641 0.00068
NM_004667.6(HERC2):c.12867C>T (p.Ile4289=) rs146760133 0.00063
NM_004667.6(HERC2):c.3987C>T (p.Val1329=) rs138699937 0.00051
NM_004667.6(HERC2):c.1704C>T (p.Ala568=) rs143388037 0.00048
NM_004667.6(HERC2):c.4651A>C (p.Ile1551Leu) rs200864382 0.00044
NM_004667.6(HERC2):c.12147G>A (p.Lys4049=) rs139351974 0.00043
NM_004667.6(HERC2):c.3749-10T>C rs191404708 0.00041
NM_004667.6(HERC2):c.3903T>A (p.Pro1301=) rs145512084 0.00035
NM_004667.6(HERC2):c.1770C>T (p.Asp590=) rs141562067 0.00032
NM_004667.6(HERC2):c.3133C>T (p.Arg1045Cys) rs117802902 0.00025
NM_004667.6(HERC2):c.3888G>T (p.Gly1296=) rs2346085 0.00024
NM_004667.6(HERC2):c.7383C>T (p.Ile2461=) rs573275628 0.00024
NM_004667.6(HERC2):c.12282C>T (p.Val4094=) rs140970725 0.00022
NM_004667.6(HERC2):c.8097A>G (p.Val2699=) rs2525937 0.00019
NM_004667.6(HERC2):c.9726C>T (p.Asp3242=) rs145255977 0.00019
NM_004667.6(HERC2):c.2463G>A (p.Pro821=) rs139813405 0.00016
NM_004667.6(HERC2):c.8329A>G (p.Met2777Val) rs184647895 0.00014
NM_004667.6(HERC2):c.2916T>C (p.Asp972=) rs370549650 0.00011
NM_004667.6(HERC2):c.9358C>T (p.Leu3120=) rs145759817 0.00011
NM_004667.6(HERC2):c.13566G>A (p.Pro4522=) rs574228980 0.00006
NM_004667.6(HERC2):c.5838T>C (p.Asp1946=) rs147592737 0.00006
NM_004667.6(HERC2):c.6615A>G (p.Ala2205=) rs78703276 0.00006
NM_004667.6(HERC2):c.11895C>T (p.Leu3965=) rs369187425 0.00004
NM_004667.6(HERC2):c.4296C>T (p.Pro1432=) rs377587657 0.00004
NM_004667.6(HERC2):c.4810-10C>T rs775084149 0.00004
NM_004667.6(HERC2):c.5448G>A (p.Thr1816=) rs753443106 0.00004
NM_004667.6(HERC2):c.6117A>G (p.Val2039=) rs2905940 0.00004
NM_004667.6(HERC2):c.8937+4C>T rs538829323 0.00004
NM_004667.6(HERC2):c.13305C>T (p.Ala4435=) rs773579592 0.00003
NM_004667.6(HERC2):c.9792C>T (p.Val3264=) rs756826766 0.00003
NM_004667.6(HERC2):c.12234G>A (p.Pro4078=) rs767672342 0.00002
NM_004667.6(HERC2):c.6009C>T (p.Ser2003=) rs780534474 0.00002
NM_004667.6(HERC2):c.1083C>T (p.His361=) rs142059352 0.00001
NM_004667.6(HERC2):c.11973C>T (p.Ile3991=) rs762974758 0.00001
NM_004667.6(HERC2):c.12750A>G (p.Lys4250=) rs774403885 0.00001
NM_004667.6(HERC2):c.14136C>T (p.Ser4712=) rs376018767 0.00001
NM_004667.6(HERC2):c.3050+8G>T rs778708768 0.00001
NM_004667.6(HERC2):c.6150G>A (p.Thr2050=) rs199593384 0.00001
NM_004667.6(HERC2):c.9180G>A (p.Thr3060=) rs754619145 0.00001
NM_004667.6(HERC2):c.9723T>C (p.Ser3241=) rs759498619 0.00001
NM_004667.6(HERC2):c.9909G>A (p.Val3303=) rs751705631 0.00001
NM_004667.6(HERC2):c.1015C>T (p.Pro339Ser)
NM_004667.6(HERC2):c.10191A>G (p.Leu3397=)
NM_004667.6(HERC2):c.10236T>C (p.Ala3412=)
NM_004667.6(HERC2):c.10239T>A (p.Val3413=)
NM_004667.6(HERC2):c.10242C>G (p.Val3414=)
NM_004667.6(HERC2):c.10260C>T (p.Ala3420=)
NM_004667.6(HERC2):c.10323G>A (p.Ala3441=)
NM_004667.6(HERC2):c.10395A>G (p.Pro3465=)
NM_004667.6(HERC2):c.10458G>A (p.Pro3486=)
NM_004667.6(HERC2):c.10530A>G (p.Ala3510=)
NM_004667.6(HERC2):c.10587G>A (p.Pro3529=)
NM_004667.6(HERC2):c.1068C>T (p.Ser356=)
NM_004667.6(HERC2):c.1074C>T (p.Gly358=)
NM_004667.6(HERC2):c.10968A>C (p.Thr3656=)
NM_004667.6(HERC2):c.10998C>T (p.Ser3666=)
NM_004667.6(HERC2):c.11009-5C>T
NM_004667.6(HERC2):c.11022C>T (p.Ser3674=)
NM_004667.6(HERC2):c.11238C>T (p.Asn3746=)
NM_004667.6(HERC2):c.1140A>G (p.Pro380=)
NM_004667.6(HERC2):c.1161T>C (p.Ile387=) rs2140987227
NM_004667.6(HERC2):c.11640C>G (p.Ala3880=)
NM_004667.6(HERC2):c.11646T>C (p.Arg3882=)
NM_004667.6(HERC2):c.11667A>G (p.Lys3889=)
NM_004667.6(HERC2):c.11835T>C (p.Thr3945=)
NM_004667.6(HERC2):c.1185T>A (p.Val395=)
NM_004667.6(HERC2):c.11991C>G (p.Leu3997=) rs1596034321
NM_004667.6(HERC2):c.12018G>A (p.Leu4006=)
NM_004667.6(HERC2):c.12072G>A (p.Ser4024=)
NM_004667.6(HERC2):c.12360C>T (p.Tyr4120=)
NM_004667.6(HERC2):c.12378C>T (p.Ser4126=)
NM_004667.6(HERC2):c.12447C>T (p.Ala4149=) rs2142165394
NM_004667.6(HERC2):c.12522C>T (p.Tyr4174=)
NM_004667.6(HERC2):c.12662+4C>T
NM_004667.6(HERC2):c.12822C>T (p.Gly4274=)
NM_004667.6(HERC2):c.12849C>T (p.Asp4283=)
NM_004667.6(HERC2):c.12933A>T (p.Ala4311=)
NM_004667.6(HERC2):c.13194G>A (p.Ala4398=)
NM_004667.6(HERC2):c.13488A>T (p.Gly4496=)
NM_004667.6(HERC2):c.13638C>T (p.Thr4546=)
NM_004667.6(HERC2):c.13707C>T (p.Ile4569=) rs762092163
NM_004667.6(HERC2):c.13919A>G (p.His4640Arg)
NM_004667.6(HERC2):c.13965C>T (p.Arg4655=)
NM_004667.6(HERC2):c.14058G>A (p.Lys4686=)
NM_004667.6(HERC2):c.1413C>T (p.Arg471=)
NM_004667.6(HERC2):c.14307C>A (p.Pro4769=)
NM_004667.6(HERC2):c.144T>C (p.Thr48=)
NM_004667.6(HERC2):c.1626C>T (p.Ser542=)
NM_004667.6(HERC2):c.165C>T (p.Asn55=)
NM_004667.6(HERC2):c.1674C>T (p.Cys558=)
NM_004667.6(HERC2):c.1782G>A (p.Pro594=)
NM_004667.6(HERC2):c.1932C>T (p.Gly644=)
NM_004667.6(HERC2):c.2088T>C (p.His696=)
NM_004667.6(HERC2):c.2250A>G (p.Pro750=)
NM_004667.6(HERC2):c.2487C>T (p.Ala829=)
NM_004667.6(HERC2):c.2643C>T (p.Thr881=)
NM_004667.6(HERC2):c.2703G>A (p.Ala901=)
NM_004667.6(HERC2):c.2742C>T (p.Cys914=)
NM_004667.6(HERC2):c.2775A>G (p.Pro925=)
NM_004667.6(HERC2):c.2812T>C (p.Leu938=) rs767399287
NM_004667.6(HERC2):c.2919A>G (p.Glu973=)
NM_004667.6(HERC2):c.323-6T>C
NM_004667.6(HERC2):c.3390T>C (p.Thr1130=)
NM_004667.6(HERC2):c.3435C>G (p.Leu1145=)
NM_004667.6(HERC2):c.3577+4C>T
NM_004667.6(HERC2):c.3948C>T (p.His1316=)
NM_004667.6(HERC2):c.3975G>A (p.Pro1325=)
NM_004667.6(HERC2):c.4095C>T (p.Ser1365=)
NM_004667.6(HERC2):c.4470G>A (p.Ser1490=)
NM_004667.6(HERC2):c.4689A>G (p.Pro1563=)
NM_004667.6(HERC2):c.4794A>G (p.Ala1598=)
NM_004667.6(HERC2):c.5679C>A (p.Arg1893=)
NM_004667.6(HERC2):c.5706A>G (p.Gly1902=)
NM_004667.6(HERC2):c.5782C>T (p.Leu1928=) rs1300122148
NM_004667.6(HERC2):c.5961C>T (p.Ser1987=)
NM_004667.6(HERC2):c.6138G>T (p.Pro2046=)
NM_004667.6(HERC2):c.6246A>G (p.Pro2082=)
NM_004667.6(HERC2):c.6373C>A (p.Arg2125=)
NM_004667.6(HERC2):c.6540A>G (p.Gly2180=)
NM_004667.6(HERC2):c.6549C>T (p.Ser2183=)
NM_004667.6(HERC2):c.6585C>T (p.Ser2195=)
NM_004667.6(HERC2):c.6729C>T (p.Thr2243=)
NM_004667.6(HERC2):c.6795C>T (p.Ala2265=)
NM_004667.6(HERC2):c.7122G>A (p.Pro2374=)
NM_004667.6(HERC2):c.7164C>T (p.Ala2388=)
NM_004667.6(HERC2):c.7518C>T (p.Ser2506=)
NM_004667.6(HERC2):c.8043C>T (p.Val2681=) rs2428639
NM_004667.6(HERC2):c.816G>A (p.Thr272=)
NM_004667.6(HERC2):c.8229C>G (p.Thr2743=) rs780136071
NM_004667.6(HERC2):c.825C>A (p.Thr275=)
NM_004667.6(HERC2):c.825C>T (p.Thr275=)
NM_004667.6(HERC2):c.8298G>A (p.Gln2766=)
NM_004667.6(HERC2):c.8508C>T (p.Ile2836=)
NM_004667.6(HERC2):c.8826-10G>T rs755016271
NM_004667.6(HERC2):c.8826-6G>T rs1418463172
NM_004667.6(HERC2):c.8868G>A (p.Thr2956=)
NM_004667.6(HERC2):c.8970A>G (p.Ser2990=)
NM_004667.6(HERC2):c.9063T>C (p.Asn3021=) rs1596139941
NM_004667.6(HERC2):c.9384C>T (p.Tyr3128=)
NM_004667.6(HERC2):c.9486C>T (p.Asp3162=)
NM_004667.6(HERC2):c.9564C>T (p.Gly3188=)
NM_004667.6(HERC2):c.9633G>A (p.Glu3211=)
NM_004667.6(HERC2):c.9813G>A (p.Ala3271=)
NM_004667.6(HERC2):c.9858C>T (p.His3286=)
NM_004667.6(HERC2):c.987C>T (p.Ser329=)

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