ClinVar Miner

List of variants in gene SNTA1 reported as uncertain significance for not provided

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Total variants: 67
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HGVS dbSNP gnomAD frequency
NM_003098.3(SNTA1):c.440C>A (p.Thr147Asn) rs141724500 0.00067
NM_003098.3(SNTA1):c.787G>T (p.Ala263Ser) rs150576530 0.00054
NM_003098.3(SNTA1):c.619C>T (p.Arg207Trp) rs139537086 0.00044
NM_003098.3(SNTA1):c.784A>C (p.Thr262Pro) rs200316080 0.00041
NM_003098.3(SNTA1):c.566C>T (p.Ser189Leu) rs144860423 0.00020
NM_003098.3(SNTA1):c.1157C>T (p.Pro386Leu) rs200865199 0.00019
NM_003098.3(SNTA1):c.1088A>C (p.Glu363Ala) rs147964932 0.00017
NM_003098.3(SNTA1):c.430T>G (p.Ser144Ala) rs142978180 0.00017
NM_003098.3(SNTA1):c.1105C>T (p.Arg369Cys) rs369968387 0.00007
NM_003098.3(SNTA1):c.589C>T (p.Arg197Trp) rs530603992 0.00006
NM_003098.3(SNTA1):c.1015C>T (p.Arg339Cys) rs138164106 0.00005
NM_003098.3(SNTA1):c.782C>T (p.Ala261Val) rs139467962 0.00005
NM_003098.3(SNTA1):c.1033G>A (p.Ala345Thr) rs150474420 0.00004
NM_003098.3(SNTA1):c.1180C>T (p.Arg394Cys) rs567451585 0.00004
NM_003098.3(SNTA1):c.556G>A (p.Gly186Ser) rs200755101 0.00004
NM_003098.3(SNTA1):c.820C>T (p.Arg274Trp) rs201763667 0.00004
NM_003098.3(SNTA1):c.992G>A (p.Arg331His) rs575431717 0.00004
NM_003098.3(SNTA1):c.160G>C (p.Gly54Arg) rs786205848 0.00003
NM_003098.3(SNTA1):c.233C>T (p.Pro78Leu) rs1241571413 0.00003
NM_003098.3(SNTA1):c.776C>T (p.Ser259Leu) rs774643587 0.00003
NM_003098.3(SNTA1):c.1109C>T (p.Thr370Met) rs746227626 0.00002
NM_003098.3(SNTA1):c.1205G>A (p.Arg402Gln) rs771369802 0.00002
NM_003098.3(SNTA1):c.1300T>C (p.Trp434Arg) rs772600822 0.00002
NM_003098.3(SNTA1):c.1324C>T (p.Arg442Ter) rs375603980 0.00002
NM_003098.3(SNTA1):c.1388T>G (p.Leu463Arg) rs188835994 0.00002
NM_003098.3(SNTA1):c.620G>A (p.Arg207Gln) rs771180054 0.00002
NM_003098.3(SNTA1):c.668C>T (p.Ser223Leu) rs779370807 0.00002
NM_003098.3(SNTA1):c.905A>G (p.Glu302Gly) rs763371307 0.00002
NM_003098.3(SNTA1):c.1151A>G (p.Glu384Gly) rs1365956176 0.00001
NM_003098.3(SNTA1):c.1169C>T (p.Ala390Val) rs121434500 0.00001
NM_003098.3(SNTA1):c.1256G>A (p.Arg419His) rs751302839 0.00001
NM_003098.3(SNTA1):c.1279A>G (p.Ile427Val) rs151158866 0.00001
NM_003098.3(SNTA1):c.1394T>C (p.Phe465Ser) rs774908810 0.00001
NM_003098.3(SNTA1):c.1425+1G>A rs113809208 0.00001
NM_003098.3(SNTA1):c.1484C>T (p.Ser495Leu) rs144006909 0.00001
NM_003098.3(SNTA1):c.200C>T (p.Ala67Val) rs536755693 0.00001
NM_003098.3(SNTA1):c.316C>T (p.Arg106Trp) rs552509775 0.00001
NM_003098.3(SNTA1):c.327G>C (p.Lys109Asn) rs1280251666 0.00001
NM_003098.3(SNTA1):c.364G>A (p.Ala122Thr) rs151113230 0.00001
NM_003098.3(SNTA1):c.375G>C (p.Gln125His) rs201421292 0.00001
NM_003098.3(SNTA1):c.403A>C (p.Ile135Leu) rs756587722 0.00001
NM_003098.3(SNTA1):c.497-5A>G rs202178576 0.00001
NM_003098.3(SNTA1):c.526T>C (p.Phe176Leu) rs781703999 0.00001
NM_003098.3(SNTA1):c.544G>A (p.Gly182Arg) rs201405395 0.00001
NM_003098.3(SNTA1):c.622A>T (p.Asn208Tyr) rs786205849 0.00001
NM_003098.3(SNTA1):c.759T>A (p.Asp253Glu) rs759487225 0.00001
NM_003098.3(SNTA1):c.773G>A (p.Arg258Lys) rs776064801 0.00001
NM_003098.3(SNTA1):c.968T>A (p.Leu323His) rs1391937955 0.00001
NM_003098.3(SNTA1):c.991C>T (p.Arg331Cys) rs769528459 0.00001
NM_003098.3(SNTA1):c.*8C>T rs1399933359
NM_003098.3(SNTA1):c.1003_1021dup (p.Ala341fs) rs775891730
NM_003098.3(SNTA1):c.1052C>T (p.Ser351Leu)
NM_003098.3(SNTA1):c.1057C>G (p.Pro353Ala) rs786205427
NM_003098.3(SNTA1):c.1127T>C (p.Val376Ala) rs1283111325
NM_003098.3(SNTA1):c.1160A>G (p.Gln387Arg)
NM_003098.3(SNTA1):c.1225G>C (p.Glu409Gln) rs786205850
NM_003098.3(SNTA1):c.1244C>T (p.Thr415Met) rs533902889
NM_003098.3(SNTA1):c.1300_1301del (p.Trp434fs) rs1273480938
NM_003098.3(SNTA1):c.1330G>A (p.Val444Met) rs201571071
NM_003098.3(SNTA1):c.1420G>A (p.Glu474Lys) rs2146754197
NM_003098.3(SNTA1):c.1456A>G (p.Ile486Val)
NM_003098.3(SNTA1):c.1498C>T (p.Arg500Cys) rs786205426
NM_003098.3(SNTA1):c.202G>A (p.Ala68Thr) rs1990629920
NM_003098.3(SNTA1):c.225dup (p.Gln76fs)
NM_003098.3(SNTA1):c.686A>G (p.Asn229Ser) rs1064796525
NM_003098.3(SNTA1):c.763G>C (p.Ala255Pro) rs1057524281
NM_003098.3(SNTA1):c.845T>A (p.Leu282Gln) rs200878531

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