ClinVar Miner

List of variants in gene SDHA reported by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 70
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HGVS dbSNP gnomAD frequency
NM_004168.4(SDHA):c.549C>T (p.Gly183=) rs61733344 0.00892
NM_004168.4(SDHA):c.17G>A (p.Gly6Asp) rs187964306 0.00596
NM_004168.4(SDHA):c.969C>T (p.Gly323=) rs142849100 0.00430
NM_004168.4(SDHA):c.1413C>T (p.Ile471=) rs34779890 0.00259
NM_004168.4(SDHA):c.1523C>T (p.Thr508Ile) rs151266052 0.00245
NM_004168.4(SDHA):c.1623G>A (p.Lys541=) rs35502109 0.00206
NM_004168.4(SDHA):c.1368G>A (p.Ser456=) rs149875171 0.00117
NM_004168.4(SDHA):c.1002G>A (p.Ala334=) rs144252500 0.00075
NM_004168.4(SDHA):c.133G>A (p.Ala45Thr) rs140736646 0.00060
NM_004168.4(SDHA):c.723C>T (p.Asp241=) rs146653693 0.00049
NM_004168.4(SDHA):c.456+6G>T rs371735891 0.00047
NM_004168.4(SDHA):c.163T>C (p.Tyr55His) rs142926807 0.00046
NM_004168.4(SDHA):c.91C>T (p.Arg31Ter) rs142441643 0.00025
NM_004168.4(SDHA):c.1569T>C (p.Ala523=) rs150192376 0.00019
NM_004168.4(SDHA):c.777C>T (p.Tyr259=) rs140243793 0.00014
NM_004168.4(SDHA):c.1979C>G (p.Ala660Gly) rs191412461 0.00013
NM_004168.4(SDHA):c.1534C>T (p.Arg512Ter) rs748089700 0.00005
NM_004168.4(SDHA):c.1014G>A (p.Ala338=) rs201341132 0.00004
NM_004168.4(SDHA):c.1526C>G (p.Ser509Trp) rs397514541 0.00004
NM_004168.4(SDHA):c.372C>T (p.Tyr124=) rs754393360 0.00004
NM_004168.4(SDHA):c.957T>C (p.Ile319=) rs757167466 0.00004
NM_004168.4(SDHA):c.1233C>T (p.Gly411=) rs376530094 0.00003
NM_004168.4(SDHA):c.1335G>A (p.Ser445=) rs200223188 0.00003
NM_004168.4(SDHA):c.512G>A (p.Arg171His) rs587782076 0.00003
NM_004168.4(SDHA):c.1356C>T (p.Leu452=) rs748496836 0.00002
NM_004168.4(SDHA):c.150C>T (p.Ser50=) rs140264486 0.00002
NM_004168.4(SDHA):c.1737C>T (p.Ile579=) rs201454617 0.00002
NM_004168.4(SDHA):c.1765C>T (p.Arg589Trp) rs387906780 0.00002
NM_004168.4(SDHA):c.1950C>T (p.Asn650=) rs1042430 0.00002
NM_004168.4(SDHA):c.598C>T (p.Leu200=) rs764307917 0.00002
NM_004168.4(SDHA):c.63+8C>T rs766358430 0.00002
NM_004168.4(SDHA):c.963T>C (p.Ser321=) rs755235011 0.00002
NM_004168.4(SDHA):c.1033C>T (p.Arg345Trp) rs760598746 0.00001
NM_004168.4(SDHA):c.1242C>T (p.Pro414=) rs777306884 0.00001
NM_004168.4(SDHA):c.1308C>T (p.Tyr436=) rs762494024 0.00001
NM_004168.4(SDHA):c.1338del (p.His447fs) rs1735791499 0.00001
NM_004168.4(SDHA):c.1340A>G (p.His447Arg) rs779151375 0.00001
NM_004168.4(SDHA):c.1410C>T (p.Ser470=) rs556476038 0.00001
NM_004168.4(SDHA):c.1430C>T (p.Pro477Leu) rs146990772 0.00001
NM_004168.4(SDHA):c.1461C>T (p.Asn487=) rs187540602 0.00001
NM_004168.4(SDHA):c.1471G>T (p.Glu491Ter) rs778207102 0.00001
NM_004168.4(SDHA):c.1753C>T (p.Arg585Trp) rs200397144 0.00001
NM_004168.4(SDHA):c.1795-3C>G rs544544409 0.00001
NM_004168.4(SDHA):c.1968C>T (p.Thr656=) rs3211499 0.00001
GRCh37/hg19 5p15.33(chr5:225534-240591)x3
NC_000005.10:g.263387C>T
NC_000005.10:g.263399G>A
NM_004168.4(SDHA):c.-7A>C rs751633537
NM_004168.4(SDHA):c.1009C>G (p.Leu337Val) rs1735560308
NM_004168.4(SDHA):c.1015T>C (p.Ser339Pro) rs1553999041
NM_004168.4(SDHA):c.1038C>A (p.Ser346=) rs1041949
NM_004168.4(SDHA):c.123G>A (p.Lys41=) rs1553997185
NM_004168.4(SDHA):c.1335G>T (p.Ser445=) rs200223188
NM_004168.4(SDHA):c.1424G>C (p.Cys475Ser) rs748567636
NM_004168.4(SDHA):c.1663+7A>G rs1579438260
NM_004168.4(SDHA):c.1766G>A (p.Arg589Gln) rs763766162
NM_004168.4(SDHA):c.1795-5C>T rs1169912956
NM_004168.4(SDHA):c.1974G>C (p.Pro658=) rs1042446
NM_004168.4(SDHA):c.222G>A (p.Leu74=)
NM_004168.4(SDHA):c.248C>T (p.Ala83Val)
NM_004168.4(SDHA):c.33G>T (p.Leu11=) rs1139423
NM_004168.4(SDHA):c.447del (p.Val150fs) rs2126547751
NM_004168.4(SDHA):c.622-13T>C
NM_004168.4(SDHA):c.667del (p.Asp223fs) rs587782077
NM_004168.4(SDHA):c.716T>C (p.Ile239Thr) rs1466069757
NM_004168.4(SDHA):c.798C>T (p.Cys266=)
NM_004168.4(SDHA):c.834C>T (p.Ala278=) rs1553998649
NM_004168.4(SDHA):c.987A>T (p.Arg329=)
NM_004168.4(SDHA):c.994C>T (p.Pro332Ser) rs373509391
NM_004168.4(SDHA):c.996T>C (p.Pro332=)

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