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New user registrations, changes to existing user profiles, and changes to user credentials will be suspended for several weeks.
This allows us to avoid multi-day, broad service outages as we continue to migrate off our current cloud hosting provider.
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 10 | g.102504153_102509303del | CA1139532141 | SUFU | c.1_317del c.8+1167_143del | |
| 10 | g.102504174_102504190del | CA2825001676 | SUFU | c.22_38del (p.Gly8ArgfsTer?) c.8+1188_8+1204del (n.8+1188_8+1204del) | ClinVar |
| 10 | g.102504189_102504205dup | CA913187385 | SUFU | c.37_53dup (p.Gly19ProfsTer?) c.8+1203_8+1219dup (n.8+1203_8+1219dup) | ClinVar dbSNP |
| 10 | g.102504189_102504205del | CA923726182 | SUFU | c.37_53del (p.Thr13TrpfsTer29) c.8+1203_8+1219del (n.8+1203_8+1219del) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 10 | g.102504188_102504194delinsCACCGCG | CA1932719193 | SUFU | c.36_42delinsCACCGCG (p.Pro12=) c.8+1202_8+1208delinsCACCGCG (n.8+1202_8+1208delinsCACCGCG) | |
| 10 | g.102504189_102504195del | CA2574656443 | SUFU | c.37_43del (p.Thr13ProfsTer?) c.8+1203_8+1209del (n.8+1203_8+1209del) | |
| 10 | g.102504189_102504194del | CA471304796 | SUFU | c.37_42del (p.Thr13_Ala14del) c.8+1203_8+1208del (n.8+1203_8+1208del) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.102504190C>A | CA377886208 | SUFU | c.38C>A (p.Thr13Asn) c.8+1204C>A (n.8+1204C>A) | dbSNP |
| 10 | g.102504190C= | CA1932719216 | SUFU | c.38C= (p.Thr13=) c.8+1204C= (n.8+1204C=) | |
| 10 | g.102504190C>G | CA5667580 | SUFU | c.38C>G (p.Thr13Ser) c.8+1204C>G (n.8+1204C>G) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 10 | g.102504190C>T | CA5667581 | SUFU | c.38C>T (p.Thr13Ile) c.8+1204C>T (n.8+1204C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.102504191C>A | CA471304797 | SUFU | c.39C>A (p.Thr13=) c.8+1205C>A (n.8+1205C>A) | gnomAD v4 |
| 10 | g.102504191C= | CA1932719224 | SUFU | c.39C= (p.Thr13=) c.8+1205C= (n.8+1205C=) | |
| 10 | g.102504191C>G | CA471304798 | SUFU | c.39C>G (p.Thr13=) c.8+1205C>G (n.8+1205C>G) | dbSNP |
| 10 | g.102504191C>T | CA471304799 | SUFU | c.39C>T (p.Thr13=) c.8+1205C>T (n.8+1205C>T) | ClinVar dbSNP gnomAD v4 |
| 10 | g.102504191_102504194delinsCGCG | CA1932719226 | SUFU | c.39_42delinsCGCG (p.Thr13=) c.8+1205_8+1208delinsCGCG (n.8+1205_8+1208delinsCGCG) | |
| 10 | g.102504191_102504215delinsCGCGCCCCCGGCCCCTGGCCCGACT | CA1932719223 | SUFU | c.39_63delinsCGCGCCCCCGGCCCCTGGCCCGACT (p.Thr13=) c.8+1205_8+1229delinsCGCGCCCCCGGCCCCTGGCCCGACT (n.8+1205_8+1229delinsCGCGCCCCCGGCCCCTGGCCCGACT) | |
| 10 | g.102504192del | CA2610694420 | SUFU | c.40del (p.Ala14ArgfsTer?) c.8+1206del (n.8+1206del) | gnomAD v4 |
| 10 | g.102504192G>A | CA377886217 | SUFU | c.40G>A (p.Ala14Thr) c.8+1206G>A (n.8+1206G>A) | ClinVar |
| 10 | g.102504192G>C | CA377886219 | SUFU | c.40G>C (p.Ala14Pro) c.8+1206G>C (n.8+1206G>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 10 | g.102504192G= | CA1932719234 | SUFU | c.40G= (p.Ala14=) c.8+1206G= (n.8+1206G=) | |
| 10 | g.102504192G>T | CA377886214 | SUFU | c.40G>T (p.Ala14Ser) c.8+1206G>T (n.8+1206G>T) | |
| 10 | g.102504192_102504194del | CA595216485 | SUFU | c.40_42del (p.Ala14del) c.8+1206_8+1208del (n.8+1206_8+1208del) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.102504194_102504217del | CA1932719233 | SUFU | c.42_65del (p.Pro15_Ala22del) c.8+1208_8+1231del (n.8+1208_8+1231del) | ClinVar dbSNP gnomAD v4 |
| 10 | g.102504193C>A | CA377886222 | SUFU | c.41C>A (p.Ala14Glu) c.8+1207C>A (n.8+1207C>A) | gnomAD v4 |
| 10 | g.102504193C>G | CA377886227 | SUFU | c.41C>G (p.Ala14Gly) c.8+1207C>G (n.8+1207C>G) | |
| 10 | g.102504193C>T | CA377886226 | SUFU | c.41C>T (p.Ala14Val) c.8+1207C>T (n.8+1207C>T) | |
| 10 | g.102504193_102504194insCCCCC | CA2610694421 | SUFU | c.41_42insCCCCC (p.Pro16ArgfsTer?) c.8+1207_8+1208insCCCCC (n.8+1207_8+1208insCCCCC) | gnomAD v4 |
| 10 | g.102504194G>A | CA471304800 | SUFU | c.42G>A (p.Ala14=) c.8+1208G>A (n.8+1208G>A) | ClinVar dbSNP gnomAD v4 |
| 10 | g.102504194G>C | CA471304801 | SUFU | c.42G>C (p.Ala14=) c.8+1208G>C (n.8+1208G>C) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.102504194G= | CA1932719239 | SUFU | c.42G= (p.Ala14=) c.8+1208G= (n.8+1208G=) | |
| 10 | g.102504194G>T | CA471304802 | SUFU | c.42G>T (p.Ala14=) c.8+1208G>T (n.8+1208G>T) | |
| 10 | g.102504194_102504218delinsGCCCCCGGCCCCTGGCCCGACTGCC | CA1932719241 | SUFU | c.42_66delinsGCCCCCGGCCCCTGGCCCGACTGCC (p.Ala14=) c.8+1208_8+1232delinsGCCCCCGGCCCCTGGCCCGACTGCC (n.8+1208_8+1232delinsGCCCCCGGCCCCTGGCCCGACTGCC) | |
| 10 | g.102504195C>A | CA5667582 | SUFU | c.43C>A (p.Pro15Thr) c.8+1209C>A (n.8+1209C>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.102504195C= | CA1932719250 | SUFU | c.43C= (p.Pro15=) c.8+1209C= (n.8+1209C=) | |
| 10 | g.102504195C>G | CA377886232 | SUFU | c.43C>G (p.Pro15Ala) c.8+1209C>G (n.8+1209C>G) | ClinVar dbSNP |
| 10 | g.102504195C>T | CA377886234 | SUFU | c.43C>T (p.Pro15Ser) c.8+1209C>T (n.8+1209C>T) | ClinVar dbSNP gnomAD v4 |
| 10 | g.102504199dup | CA2610694422 | SUFU | c.47dup (p.Ala17GlyfsTer?) c.8+1213dup (n.8+1213dup) | gnomAD v4 |
| 10 | g.102504199del | CA2574656482 | SUFU | c.47del (p.Pro16ArgfsTer?) c.8+1213del (n.8+1213del) | dbSNP gnomAD v4 |
| 10 | g.102504204_102504227del | CA659052198 | SUFU | c.52_75del (p.Pro18_Ala25del) c.8+1218_8+1241del (n.8+1218_8+1241del) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 10 | g.102504196C>A | CA377886238 | SUFU | c.44C>A (p.Pro15His) c.8+1210C>A (n.8+1210C>A) | gnomAD v4 |
| 10 | g.102504196C= | CA1932719258 | SUFU | c.44C= (p.Pro15=) c.8+1210C= (n.8+1210C=) | |
| 10 | g.102504196C>G | CA377886241 | SUFU | c.44C>G (p.Pro15Arg) c.8+1210C>G (n.8+1210C>G) | |
| 10 | g.102504196C>T | CA116361 | SUFU | c.44C>T (p.Pro15Leu) c.8+1210C>T (n.8+1210C>T) | ClinVar dbSNP |
| 10 | g.102504197C>A | CA471304804 | SUFU | c.45C>A (p.Pro15=) c.8+1211C>A (n.8+1211C>A) | ClinVar gnomAD v4 |
| 10 | g.102504197C= | CA1932719262 | SUFU | c.45C= (p.Pro15=) c.8+1211C= (n.8+1211C=) | |
| 10 | g.102504197C>G | CA471304803 | SUFU | c.45C>G (p.Pro15=) c.8+1211C>G (n.8+1211C>G) | |
| 10 | g.102504197C>T | CA5667583 | SUFU | c.45C>T (p.Pro15=) c.8+1211C>T (n.8+1211C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 10 | g.102504198C>A | CA212238099 | SUFU | c.46C>A (p.Pro16Thr) c.8+1212C>A (n.8+1212C>A) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.102504198C= | CA1932719268 | SUFU | c.46C= (p.Pro16=) c.8+1212C= (n.8+1212C=) | |
| 10 | g.102504198C>G | CA377886246 | SUFU | c.46C>G (p.Pro16Ala) c.8+1212C>G (n.8+1212C>G) | ClinVar |
| 10 | g.102504198C>T | CA377886248 | SUFU | c.46C>T (p.Pro16Ser) c.8+1212C>T (n.8+1212C>T) | dbSNP gnomAD v3 gnomAD v4 |
| 10 | g.102504199C>A | CA377886251 | SUFU | c.47C>A (p.Pro16Gln) c.8+1213C>A (n.8+1213C>A) | gnomAD v4 |
| 10 | g.102504199C= | CA1932719276 | SUFU | c.47C= (p.Pro16=) c.8+1213C= (n.8+1213C=) | |
| 10 | g.102504199C>G | CA377886250 | SUFU | c.47C>G (p.Pro16Arg) c.8+1213C>G (n.8+1213C>G) | |
| 10 | g.102504199C>T | CA377886249 | SUFU | c.47C>T (p.Pro16Leu) c.8+1213C>T (n.8+1213C>T) | ClinVar dbSNP gnomAD v4 |
| 10 | g.102504199_102504201delinsCGG | CA1932719274 | SUFU | c.47_49delinsCGG (p.Pro16=) c.8+1213_8+1215delinsCGG (n.8+1213_8+1215delinsCGG) | |
| 10 | g.102504199_102504200insCCCCCCCG | CA2610694423 | SUFU | c.47_48insCCCCCCCG (p.Ala17ProfsTer?) c.8+1213_8+1214insCCCCCCCG (n.8+1213_8+1214insCCCCCCCG) | gnomAD v4 |
| 10 | g.102504200G>A | CA471304805 | SUFU | c.48G>A (p.Pro16=) c.8+1214G>A (n.8+1214G>A) | dbSNP gnomAD v4 |
| 10 | g.102504200G>C | CA471304806 | SUFU | c.48G>C (p.Pro16=) c.8+1214G>C (n.8+1214G>C) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.102504200G= | CA1932719281 | SUFU | c.48G= (p.Pro16=) c.8+1214G= (n.8+1214G=) | |
| 10 | g.102504200G>T | CA471304807 | SUFU | c.48G>T (p.Pro16=) c.8+1214G>T (n.8+1214G>T) | ClinVar dbSNP |
| 10 | g.102504200_102504201del | CA595216486 | SUFU | c.48_49del (p.Ala17ProfsTer?) c.8+1214_8+1215del (n.8+1214_8+1215del) | dbSNP gnomAD v2 gnomAD v4 |
| 10 | g.102504201del | CA2610694424 | SUFU | c.49del (p.Ala17ProfsTer?) c.8+1215del (n.8+1215del) | gnomAD v4 |
| 10 | g.102504205_102504211del | CA2573145476 | SUFU | c.53_59del (p.Pro18ArgfsTer?) c.8+1219_8+1225del (n.8+1219_8+1225del) | ClinVar dbSNP |
| 10 | g.102504201G>A | CA377886252 | SUFU | c.49G>A (p.Ala17Thr) c.8+1215G>A (n.8+1215G>A) | gnomAD v4 |
| 10 | g.102504201G>C | CA377886254 | SUFU | c.49G>C (p.Ala17Pro) c.8+1215G>C (n.8+1215G>C) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.102504201G= | CA1932719285 | SUFU | c.49G= (p.Ala17=) c.8+1215G= (n.8+1215G=) | |
| 10 | g.102504201G>T | CA377886256 | SUFU | c.49G>T (p.Ala17Ser) c.8+1215G>T (n.8+1215G>T) | gnomAD v4 |
| 10 | g.102504202C>A | CA377886259 | SUFU | c.50C>A (p.Ala17Asp) c.8+1216C>A (n.8+1216C>A) | dbSNP |
| 10 | g.102504202C= | CA1932719295 | SUFU | c.50C= (p.Ala17=) c.8+1216C= (n.8+1216C=) | |
| 10 | g.102504202C>G | CA377886260 | SUFU | c.50C>G (p.Ala17Gly) c.8+1216C>G (n.8+1216C>G) | ClinVar gnomAD v4 |
| 10 | g.102504202C>T | CA5667584 | SUFU | c.50C>T (p.Ala17Val) c.8+1216C>T (n.8+1216C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 10 | g.102504205del | CA2573145477 | SUFU | c.53del (p.Pro18LeufsTer?) c.8+1219del (n.8+1219del) | ClinVar dbSNP |
| 10 | g.102504203C>A | CA471304808 | SUFU | c.51C>A (p.Ala17=) c.8+1217C>A (n.8+1217C>A) | dbSNP |
| 10 | g.102504203C= | CA1932719298 | SUFU | c.51C= (p.Ala17=) c.8+1217C= (n.8+1217C=) | |
| 10 | g.102504203C>G | CA471304809 | SUFU | c.51C>G (p.Ala17=) c.8+1217C>G (n.8+1217C>G) | |
| 10 | g.102504203C>T | CA471304810 | SUFU | c.51C>T (p.Ala17=) c.8+1217C>T (n.8+1217C>T) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 10 | g.102504204C>A | CA377886265 | SUFU | c.52C>A (p.Pro18Thr) c.8+1218C>A (n.8+1218C>A) | ClinVar gnomAD v4 |
| 10 | g.102504204C= | CA1932719301 | SUFU | c.52C= (p.Pro18=) c.8+1218C= (n.8+1218C=) | |
| 10 | g.102504204C>G | CA377886267 | SUFU | c.52C>G (p.Pro18Ala) c.8+1218C>G (n.8+1218C>G) | ClinVar |
| 10 | g.102504204C>T | CA377886268 | SUFU | c.52C>T (p.Pro18Ser) c.8+1218C>T (n.8+1218C>T) | dbSNP gnomAD v4 |
| 10 | g.102504206_102504210del | CA2610694425 | SUFU | c.54_58del (p.Gly19AspfsTer27) c.8+1220_8+1224del (n.8+1220_8+1224del) | gnomAD v4 |
| 10 | g.102504205C>A | CA377886270 | SUFU | c.53C>A (p.Pro18His) c.8+1219C>A (n.8+1219C>A) | |
| 10 | g.102504205C= | CA1932719307 | SUFU | c.53C= (p.Pro18=) c.8+1219C= (n.8+1219C=) | |
| 10 | g.102504205C>G | CA377886271 | SUFU | c.53C>G (p.Pro18Arg) c.8+1219C>G (n.8+1219C>G) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 10 | g.102504205C>T | CA377886273 | SUFU | c.53C>T (p.Pro18Leu) c.8+1219C>T (n.8+1219C>T) | ClinVar |
| 10 | g.102504206_102504209del | CA2610694426 | SUFU | c.54_57del (p.Gly19ArgfsTer?) c.8+1220_8+1223del (n.8+1220_8+1223del) | gnomAD v4 |
| 10 | g.102504206T>A | CA471304811 | SUFU | c.54T>A (p.Pro18=) c.8+1220T>A (n.8+1220T>A) | ClinVar gnomAD v4 |
| 10 | g.102504206T>C | CA471304812 | SUFU | c.54T>C (p.Pro18=) c.8+1220T>C (n.8+1220T>C) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.102504206T>G | CA471304813 | SUFU | c.54T>G (p.Pro18=) c.8+1220T>G (n.8+1220T>G) | gnomAD v4 |
| 10 | g.102504206T= | CA1932719312 | SUFU | c.54T= (p.Pro18=) c.8+1220T= (n.8+1220T=) | |
| 10 | g.102504206_102504208del | CA2610694427 | SUFU | c.54_56del (p.Gly19del) c.8+1220_8+1222del (n.8+1220_8+1222del) | dbSNP gnomAD v4 |
| 10 | g.102504206_102504213del | CA2610694428 | SUFU | c.54_61del (p.Gly19CysfsTer26) c.8+1220_8+1227del (n.8+1220_8+1227del) | gnomAD v4 |
| 10 | g.102504206_102504216del | CA2610694429 | SUFU | c.54_64del (p.Gly19ProfsTer25) c.8+1220_8+1230del (n.8+1220_8+1230del) | dbSNP gnomAD v4 |
| 10 | g.102504207G>A | CA377886277 | SUFU | c.55G>A (p.Gly19Ser) c.8+1221G>A (n.8+1221G>A) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 10 | g.102504207G>C | CA377886279 | SUFU | c.55G>C (p.Gly19Arg) c.8+1221G>C (n.8+1221G>C) | dbSNP gnomAD v4 |
| 10 | g.102504207G= | CA1932719319 | SUFU | c.55G= (p.Gly19=) c.8+1221G= (n.8+1221G=) | |
| 10 | g.102504207G>T | CA377886275 | SUFU | c.55G>T (p.Gly19Cys) c.8+1221G>T (n.8+1221G>T) | gnomAD v4 |
| 10 | g.102504207_102504221dup | CA2740093513 | SUFU | c.55_69dup (p.Pro23_Pro24insGlyProThrAlaPro) c.8+1221_8+1235dup (n.8+1221_8+1235dup) | ClinVar |
| 10 | g.102504208G>A | CA377886281 | SUFU | c.56G>A (p.Gly19Asp) c.8+1222G>A (n.8+1222G>A) | ClinVar dbSNP |
| 10 | g.102504208G>C | CA377886284 | SUFU | c.56G>C (p.Gly19Ala) c.8+1222G>C (n.8+1222G>C) | dbSNP |
| 10 | g.102504208G= | CA1932719325 | SUFU | c.56G= (p.Gly19=) c.8+1222G= (n.8+1222G=) | |
| 10 | g.102504208G>T | CA377886286 | SUFU | c.56G>T (p.Gly19Val) c.8+1222G>T (n.8+1222G>T) | ClinVar |
| 10 | g.102504209C>A | CA471304814 | SUFU | c.57C>A (p.Gly19=) c.8+1223C>A (n.8+1223C>A) | ClinVar |
| 10 | g.102504209C>G | CA471304815 | SUFU | c.57C>G (p.Gly19=) c.8+1223C>G (n.8+1223C>G) | |
| 10 | g.102504209C>T | CA471304816 | SUFU | c.57C>T (p.Gly19=) c.8+1223C>T (n.8+1223C>T) | ClinVar dbSNP |
| 10 | g.102504209_102504215del | CA2610694430 | SUFU | c.57_63del (p.Thr21ProfsTer?) c.8+1223_8+1229del (n.8+1223_8+1229del) | gnomAD v4 |
| 10 | g.102504212_102504220del | CA2610694431 | SUFU | c.60_68del (p.Thr21_Pro23del) c.8+1226_8+1234del (n.8+1226_8+1234del) | gnomAD v4 |
| 10 | g.102504210C>A | CA377886287 | SUFU | c.58C>A (p.Pro20Thr) c.8+1224C>A (n.8+1224C>A) | |
| 10 | g.102504210C= | CA1932719330 | SUFU | c.58C= (p.Pro20=) c.8+1224C= (n.8+1224C=) | |
| 10 | g.102504210C>G | CA212238100 | SUFU | c.58C>G (p.Pro20Ala) c.8+1224C>G (n.8+1224C>G) | ClinVar dbSNP |
| 10 | g.102504210C>T | CA377886290 | SUFU | c.58C>T (p.Pro20Ser) c.8+1224C>T (n.8+1224C>T) | dbSNP gnomAD v2 gnomAD v4 |
| 10 | g.102504211C>A | CA377886291 | SUFU | c.59C>A (p.Pro20Gln) c.8+1225C>A (n.8+1225C>A) | |
| 10 | g.102504211C>G | CA377886294 | SUFU | c.59C>G (p.Pro20Arg) c.8+1225C>G (n.8+1225C>G) | ClinVar gnomAD v4 |
| 10 | g.102504211C>T | CA377886296 | SUFU | c.59C>T (p.Pro20Leu) c.8+1225C>T (n.8+1225C>T) | ClinVar |
| 10 | g.102504211_102504215del | CA2610694432 | SUFU | c.59_63del (p.Pro20ArgfsTer26) c.8+1225_8+1229del (n.8+1225_8+1229del) | gnomAD v4 |
| 10 | g.102504212_102504217del | CA2722591405 | SUFU | c.60_65del (p.Thr21_Ala22del) c.8+1226_8+1231del (n.8+1226_8+1231del) | dbSNP |
| 10 | g.102504212G>A | CA471304817 | SUFU | c.60G>A (p.Pro20=) c.8+1226G>A (n.8+1226G>A) | ClinVar |
| 10 | g.102504212G>C | CA471304818 | SUFU | c.60G>C (p.Pro20=) c.8+1226G>C (n.8+1226G>C) | ClinVar dbSNP gnomAD v4 |
| 10 | g.102504212G= | CA1932719336 | SUFU | c.60G= (p.Pro20=) c.8+1226G= (n.8+1226G=) | |
| 10 | g.102504212G>T | CA471304819 | SUFU | c.60G>T (p.Pro20=) c.8+1226G>T (n.8+1226G>T) | ClinVar dbSNP gnomAD v4 |
| 10 | g.102504212_102504216del | CA2610694433 | SUFU | c.60_64del (p.Thr21ProfsTer25) c.8+1226_8+1230del (n.8+1226_8+1230del) | dbSNP gnomAD v4 |
| 10 | g.102504213A>C | CA377886298 | SUFU | c.61A>C (p.Thr21Pro) c.8+1227A>C (n.8+1227A>C) | dbSNP gnomAD v4 |
| 10 | g.102504213A>G | CA377886301 | SUFU | c.61A>G (p.Thr21Ala) c.8+1227A>G (n.8+1227A>G) | dbSNP gnomAD v4 |
| 10 | g.102504213A>T | CA377886303 | SUFU | c.61A>T (p.Thr21Ser) c.8+1227A>T (n.8+1227A>T) | dbSNP |
| 10 | g.102504213_102504215del | CA2610694434 | SUFU | c.61_63del (p.Thr21del) c.8+1227_8+1229del (n.8+1227_8+1229del) | gnomAD v4 |
| 10 | g.102504213_102504217del | CA2610694435 | SUFU | c.61_65del (p.Thr21ProfsTer25) c.8+1227_8+1231del (n.8+1227_8+1231del) | gnomAD v4 |
| 10 | g.102504214C>A | CA377886308 | SUFU | c.62C>A (p.Thr21Asn) c.8+1228C>A (n.8+1228C>A) | gnomAD v4 |
| 10 | g.102504214C>G | CA377886312 | SUFU | c.62C>G (p.Thr21Ser) c.8+1228C>G (n.8+1228C>G) | |
| 10 | g.102504214C>T | CA377886306 | SUFU | c.62C>T (p.Thr21Ile) c.8+1228C>T (n.8+1228C>T) | ClinVar |
| 10 | g.102504215T>A | CA471304820 | SUFU | c.63T>A (p.Thr21=) c.8+1229T>A (n.8+1229T>A) | gnomAD v4 COSMIC |
| 10 | g.102504215T>C | CA471304821 | SUFU | c.63T>C (p.Thr21=) c.8+1229T>C (n.8+1229T>C) | ClinVar dbSNP gnomAD v4 |
| 10 | g.102504215T>G | CA471304822 | SUFU | c.63T>G (p.Thr21=) c.8+1229T>G (n.8+1229T>G) | ClinVar |
| 10 | g.102504215T= | CA1932719342 | SUFU | c.63T= (p.Thr21=) c.8+1229T= (n.8+1229T=) | |
| 10 | g.102504216G>A | CA377886314 | SUFU | c.64G>A (p.Ala22Thr) c.8+1230G>A (n.8+1230G>A) | |
| 10 | g.102504216G>C | CA377886318 | SUFU | c.64G>C (p.Ala22Pro) c.8+1230G>C (n.8+1230G>C) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 10 | g.102504216G= | CA1932719347 | SUFU | c.64G= (p.Ala22=) c.8+1230G= (n.8+1230G=) | |
| 10 | g.102504216G>T | CA377886319 | SUFU | c.64G>T (p.Ala22Ser) c.8+1230G>T (n.8+1230G>T) | ClinVar gnomAD v4 |
| 10 | g.102504216_102504217delinsGC | CA1932719345 | SUFU | c.64_65delinsGC (p.Ala22=) c.8+1230_8+1231delinsGC (n.8+1230_8+1231delinsGC) | |
| 10 | g.102504217C>A | CA377886325 | SUFU | c.65C>A (p.Ala22Asp) c.8+1231C>A (n.8+1231C>A) | ClinVar dbSNP gnomAD v4 |
| 10 | g.102504217C= | CA1932719355 | SUFU | c.65C= (p.Ala22=) c.8+1231C= (n.8+1231C=) | |
| 10 | g.102504217C>G | CA5667586 | SUFU | c.65C>G (p.Ala22Gly) c.8+1231C>G (n.8+1231C>G) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.102504217C>T | CA212238105 | SUFU | c.65C>T (p.Ala22Val) c.8+1231C>T (n.8+1231C>T) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 10 | g.102504223dup | CA5667585 | SUFU | c.71dup (p.Ala25GlyfsTer23) c.8+1237dup (n.8+1237dup) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 10 | g.102504222_102504223dup | CA2789277812 | SUFU | c.70_71dup (p.Ala25ArgfsTer?) c.8+1236_8+1237dup (n.8+1236_8+1237dup) | |
| 10 | g.102504223del | CA116365 | SUFU | c.71del (p.Pro24ArgfsTer?) c.8+1237del (n.8+1237del) | ClinVar dbSNP gnomAD v4 COSMIC |
| 10 | g.102504218C>A | CA471304823 | SUFU | c.66C>A (p.Ala22=) c.8+1232C>A (n.8+1232C>A) | ClinVar dbSNP |
| 10 | g.102504218C= | CA1932719360 | SUFU | c.66C= (p.Ala22=) c.8+1232C= (n.8+1232C=) | |
| 10 | g.102504218C>G | CA471304824 | SUFU | c.66C>G (p.Ala22=) c.8+1232C>G (n.8+1232C>G) | ClinVar dbSNP gnomAD v4 |
| 10 | g.102504218C>T | CA471304825 | SUFU | c.66C>T (p.Ala22=) c.8+1232C>T (n.8+1232C>T) | ClinVar dbSNP gnomAD v4 |
| 10 | g.102504219C>A | CA377886327 | SUFU | c.67C>A (p.Pro23Thr) c.8+1233C>A (n.8+1233C>A) | |
| 10 | g.102504219C= | CA1932719363 | SUFU | c.67C= (p.Pro23=) c.8+1233C= (n.8+1233C=) | |
| 10 | g.102504219C>G | CA377886330 | SUFU | c.67C>G (p.Pro23Ala) c.8+1233C>G (n.8+1233C>G) | ClinVar dbSNP |
| 10 | g.102504219C>T | CA5667587 | SUFU | c.67C>T (p.Pro23Ser) c.8+1233C>T (n.8+1233C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.102504220C>A | CA377886333 | SUFU | c.68C>A (p.Pro23His) c.8+1234C>A (n.8+1234C>A) | |
| 10 | g.102504220C= | CA1932719368 | SUFU | c.68C= (p.Pro23=) c.8+1234C= (n.8+1234C=) | |
| 10 | g.102504220C>G | CA377886336 | SUFU | c.68C>G (p.Pro23Arg) c.8+1234C>G (n.8+1234C>G) | ClinVar |
| 10 | g.102504220C>T | CA377886338 | SUFU | c.68C>T (p.Pro23Leu) c.8+1234C>T (n.8+1234C>T) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 10 | g.102504221C>A | CA471304826 | SUFU | c.69C>A (p.Pro23=) c.8+1235C>A (n.8+1235C>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.102504221C= | CA1932719372 | SUFU | c.69C= (p.Pro23=) c.8+1235C= (n.8+1235C=) | |
| 10 | g.102504221C>G | CA471304827 | SUFU | c.69C>G (p.Pro23=) c.8+1235C>G (n.8+1235C>G) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 10 | g.102504221C>T | CA471304828 | SUFU | c.69C>T (p.Pro23=) c.8+1235C>T (n.8+1235C>T) | ClinVar dbSNP gnomAD v4 |
| 10 | g.102504222C>A | CA377886340 | SUFU | c.70C>A (p.Pro24Thr) c.8+1236C>A (n.8+1236C>A) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 10 | g.102504222C= | CA1932719381 | SUFU | c.70C= (p.Pro24=) c.8+1236C= (n.8+1236C=) | |
| 10 | g.102504222C>G | CA377886343 | SUFU | c.70C>G (p.Pro24Ala) c.8+1236C>G (n.8+1236C>G) | ClinVar dbSNP |
| 10 | g.102504222C>T | CA377886342 | SUFU | c.70C>T (p.Pro24Ser) c.8+1236C>T (n.8+1236C>T) | ClinVar dbSNP |
| 10 | g.102504223C>A | CA377886345 | SUFU | c.71C>A (p.Pro24Gln) c.8+1237C>A (n.8+1237C>A) | ClinVar dbSNP gnomAD v4 |
| 10 | g.102504223C= | CA1932719382 | SUFU | c.71C= (p.Pro24=) c.8+1237C= (n.8+1237C=) | |
| 10 | g.102504223C>G | CA377886347 | SUFU | c.71C>G (p.Pro24Arg) c.8+1237C>G (n.8+1237C>G) | |
| 10 | g.102504223C>T | CA5667588 | SUFU | c.71C>T (p.Pro24Leu) c.8+1237C>T (n.8+1237C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 10 | g.102504224G>A | CA471304831 | SUFU | c.72G>A (p.Pro24=) c.8+1238G>A (n.8+1238G>A) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 10 | g.102504224G>C | CA471304829 | SUFU | c.72G>C (p.Pro24=) c.8+1238G>C (n.8+1238G>C) | ClinVar dbSNP gnomAD v4 |
| 10 | g.102504224G= | CA1932719386 | SUFU | c.72G= (p.Pro24=) c.8+1238G= (n.8+1238G=) | |
| 10 | g.102504224G>T | CA471304830 | SUFU | c.72G>T (p.Pro24=) c.8+1238G>T (n.8+1238G>T) | |
| 10 | g.102504225dup | CA2573145479 | SUFU | c.73dup (p.Ala25GlyfsTer23) c.8+1239dup (n.8+1239dup) | ClinVar dbSNP |
| 10 | g.102504225G>A | CA377886349 | SUFU | c.73G>A (p.Ala25Thr) c.8+1239G>A (n.8+1239G>A) | ClinVar dbSNP |
| 10 | g.102504225G>C | CA377886351 | SUFU | c.73G>C (p.Ala25Pro) c.8+1239G>C (n.8+1239G>C) | dbSNP |
| 10 | g.102504225G>T | CA377886353 | SUFU | c.73G>T (p.Ala25Ser) c.8+1239G>T (n.8+1239G>T) | |
| 10 | g.102504226C>A | CA377886355 | SUFU | c.74C>A (p.Ala25Asp) c.8+1240C>A (n.8+1240C>A) | |
| 10 | g.102504226C= | CA1932719388 | SUFU | c.74C= (p.Ala25=) c.8+1240C= (n.8+1240C=) | |
| 10 | g.102504226C>G | CA377886357 | SUFU | c.74C>G (p.Ala25Gly) c.8+1240C>G (n.8+1240C>G) | |
| 10 | g.102504226C>T | CA377886358 | SUFU | c.74C>T (p.Ala25Val) c.8+1240C>T (n.8+1240C>T) | ClinVar dbSNP |
| 10 | g.102504227C>A | CA471304832 | SUFU | c.75C>A (p.Ala25=) c.8+1241C>A (n.8+1241C>A) | |
| 10 | g.102504227C= | CA1932719390 | SUFU | c.75C= (p.Ala25=) c.8+1241C= (n.8+1241C=) | |
| 10 | g.102504227C>G | CA212238157 | SUFU | c.75C>G (p.Ala25=) c.8+1241C>G (n.8+1241C>G) | dbSNP |
| 10 | g.102504227C>T | CA471304833 | SUFU | c.75C>T (p.Ala25=) c.8+1241C>T (n.8+1241C>T) | |
| 10 | g.102504234_102504238del | CA2580616857 | SUFU | c.82_86del (p.Ser28LeufsTer18) c.8+1248_8+1252del (n.8+1248_8+1252del) | ClinVar dbSNP |
| 10 | g.102504228T>A | CA377886361 | SUFU | c.76T>A (p.Phe26Ile) c.8+1242T>A (n.8+1242T>A) | ClinVar |
| 10 | g.102504228T>C | CA377886362 | SUFU | c.76T>C (p.Phe26Leu) c.8+1242T>C (n.8+1242T>C) | dbSNP gnomAD v4 |
| 10 | g.102504228T>G | CA377886364 | SUFU | c.76T>G (p.Phe26Val) c.8+1242T>G (n.8+1242T>G) | |
| 10 | g.102504228T= | CA1932719393 | SUFU | c.76T= (p.Phe26=) c.8+1242T= (n.8+1242T=) | |
| 10 | g.102504229T>A | CA377886366 | SUFU | c.77T>A (p.Phe26Tyr) c.8+1243T>A (n.8+1243T>A) | |
| 10 | g.102504229T>C | CA377886368 | SUFU | c.77T>C (p.Phe26Ser) c.8+1243T>C (n.8+1243T>C) | dbSNP |
| 10 | g.102504229T>G | CA377886370 | SUFU | c.77T>G (p.Phe26Cys) c.8+1243T>G (n.8+1243T>G) | |
| 10 | g.102504230C>A | CA377886372 | SUFU | c.78C>A (p.Phe26Leu) c.8+1244C>A (n.8+1244C>A) | |
| 10 | g.102504230C>G | CA377886374 | SUFU | c.78C>G (p.Phe26Leu) c.8+1244C>G (n.8+1244C>G) | dbSNP |
| 10 | g.102504230C>T | CA471304834 | SUFU | c.78C>T (p.Phe26=) c.8+1244C>T (n.8+1244C>T) | ClinVar dbSNP |
| 10 | g.102504231G>A | CA377886376 | SUFU | c.79G>A (p.Ala27Thr) c.8+1245G>A (n.8+1245G>A) | ClinVar dbSNP gnomAD v4 |
| 10 | g.102504231G>C | CA377886378 | SUFU | c.79G>C (p.Ala27Pro) c.8+1245G>C (n.8+1245G>C) | dbSNP |
| 10 | g.102504231G= | CA1932719398 | SUFU | c.79G= (p.Ala27=) c.8+1245G= (n.8+1245G=) | |
| 10 | g.102504231G>T | CA377886380 | SUFU | c.79G>T (p.Ala27Ser) c.8+1245G>T (n.8+1245G>T) | |
| 10 | g.102504232C>A | CA377886383 | SUFU | c.80C>A (p.Ala27Asp) c.8+1246C>A (n.8+1246C>A) | dbSNP gnomAD v3 gnomAD v4 |
| 10 | g.102504232C= | CA1932719405 | SUFU | c.80C= (p.Ala27=) c.8+1246C= (n.8+1246C=) | |
| 10 | g.102504232C>G | CA377886384 | SUFU | c.80C>G (p.Ala27Gly) c.8+1246C>G (n.8+1246C>G) | |
| 10 | g.102504232C>T | CA377886386 | SUFU | c.80C>T (p.Ala27Val) c.8+1246C>T (n.8+1246C>T) | ClinVar dbSNP |
| 10 | g.102504233T>A | CA471304835 | SUFU | c.81T>A (p.Ala27=) c.8+1247T>A (n.8+1247T>A) | |
| 10 | g.102504233T>C | CA471304836 | SUFU | c.81T>C (p.Ala27=) c.8+1247T>C (n.8+1247T>C) | ClinVar |
| 10 | g.102504233T>G | CA471304837 | SUFU | c.81T>G (p.Ala27=) c.8+1247T>G (n.8+1247T>G) | ClinVar |
| 10 | g.102504234T>A | CA377886389 | SUFU | c.82T>A (p.Ser28Thr) c.8+1248T>A (n.8+1248T>A) | |
| 10 | g.102504234T>C | CA377886390 | SUFU | c.82T>C (p.Ser28Pro) c.8+1248T>C (n.8+1248T>C) | |
| 10 | g.102504234T>G | CA377886392 | SUFU | c.82T>G (p.Ser28Ala) c.8+1248T>G (n.8+1248T>G) | ClinVar |
| 10 | g.102504235C>A | CA377886395 | SUFU | c.83C>A (p.Ser28Ter) c.8+1249C>A (n.8+1249C>A) | dbSNP |
| 10 | g.102504235C= | CA1932719407 | SUFU | c.83C= (p.Ser28=) c.8+1249C= (n.8+1249C=) | |
| 10 | g.102504235C>G | CA377886396 | SUFU | c.83C>G (p.Ser28Trp) c.8+1249C>G (n.8+1249C>G) | |
| 10 | g.102504235C>T | CA5667589 | SUFU | c.83C>T (p.Ser28Leu) c.8+1249C>T (n.8+1249C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.102504236G>A | CA5667591 | SUFU | c.84G>A (p.Ser28=) c.8+1250G>A (n.8+1250G>A) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 10 | g.102504236G>C | CA471304838 | SUFU | c.84G>C (p.Ser28=) c.8+1250G>C (n.8+1250G>C) | ClinVar dbSNP |
| 10 | g.102504236G= | CA1932719416 | SUFU | c.84G= (p.Ser28=) c.8+1250G= (n.8+1250G=) | |
| 10 | g.102504236G>T | CA5667590 | SUFU | c.84G>T (p.Ser28=) c.8+1250G>T (n.8+1250G>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.102504237C>A | CA377886402 | SUFU | c.85C>A (p.Leu29Ile) c.8+1251C>A (n.8+1251C>A) | |
| 10 | g.102504237C>G | CA377886404 | SUFU | c.85C>G (p.Leu29Val) c.8+1251C>G (n.8+1251C>G) | |
| 10 | g.102504237C>T | CA377886405 | SUFU | c.85C>T (p.Leu29Phe) c.8+1251C>T (n.8+1251C>T) | |
| 10 | g.102504239_102504240del | CA2740093514 | SUFU | c.87_88del (p.Phe30SerfsTer17) c.8+1253_8+1254del (n.8+1253_8+1254del) | ClinVar |
| 10 | g.102504238T>A | CA377886408 | SUFU | c.86T>A (p.Leu29His) c.8+1252T>A (n.8+1252T>A) | |
| 10 | g.102504238T>C | CA377886409 | SUFU | c.86T>C (p.Leu29Pro) c.8+1252T>C (n.8+1252T>C) | COSMIC |
| 10 | g.102504238T>G | CA377886411 | SUFU | c.86T>G (p.Leu29Arg) c.8+1252T>G (n.8+1252T>G) | ClinVar dbSNP gnomAD v4 |
| 10 | g.102504238T= | CA1932719428 | SUFU | c.86T= (p.Leu29=) c.8+1252T= (n.8+1252T=) | |
| 10 | g.102504239C>A | CA471304841 | SUFU | c.87C>A (p.Leu29=) c.8+1253C>A (n.8+1253C>A) | |
| 10 | g.102504239C>G | CA471304839 | SUFU | c.87C>G (p.Leu29=) c.8+1253C>G (n.8+1253C>G) | gnomAD v4 |
| 10 | g.102504239C>T | CA471304840 | SUFU | c.87C>T (p.Leu29=) c.8+1253C>T (n.8+1253C>T) | ClinVar dbSNP gnomAD v4 |
| 10 | g.102504240T>A | CA377886417 | SUFU | c.88T>A (p.Phe30Ile) c.8+1254T>A (n.8+1254T>A) | |
| 10 | g.102504240T>C | CA377886414 | SUFU | c.88T>C (p.Phe30Leu) c.8+1254T>C (n.8+1254T>C) | dbSNP gnomAD v4 |
| 10 | g.102504240T>G | CA377886416 | SUFU | c.88T>G (p.Phe30Val) c.8+1254T>G (n.8+1254T>G) | |
| 10 | g.102504242dup | CA2722591904 | SUFU | c.90dup (p.Pro31SerfsTer17) c.8+1256dup (n.8+1256dup) | dbSNP |
| 10 | g.102504241T>A | CA377886419 | SUFU | c.89T>A (p.Phe30Tyr) c.8+1255T>A (n.8+1255T>A) | |
| 10 | g.102504241T>C | CA377886421 | SUFU | c.89T>C (p.Phe30Ser) c.8+1255T>C (n.8+1255T>C) | dbSNP |
| 10 | g.102504241T>G | CA377886423 | SUFU | c.89T>G (p.Phe30Cys) c.8+1255T>G (n.8+1255T>G) | gnomAD v4 |
| 10 | g.102504242T>A | CA377886425 | SUFU | c.90T>A (p.Phe30Leu) c.8+1256T>A (n.8+1256T>A) | |
| 10 | g.102504242T>C | CA471304842 | SUFU | c.90T>C (p.Phe30=) c.8+1256T>C (n.8+1256T>C) | ClinVar dbSNP gnomAD v4 |
| 10 | g.102504242T>G | CA377886427 | SUFU | c.90T>G (p.Phe30Leu) c.8+1256T>G (n.8+1256T>G) | |
| 10 | g.102504242T= | CA1932719436 | SUFU | c.90T= (p.Phe30=) c.8+1256T= (n.8+1256T=) | |
| 10 | g.102504243C>A | CA377886432 | SUFU | c.91C>A (p.Pro31Thr) c.8+1257C>A (n.8+1257C>A) | ClinVar dbSNP gnomAD v4 |
| 10 | g.102504243C= | CA1932719440 | SUFU | c.91C= (p.Pro31=) c.8+1257C= (n.8+1257C=) | |
| 10 | g.102504243C>G | CA377886429 | SUFU | c.91C>G (p.Pro31Ala) c.8+1257C>G (n.8+1257C>G) | ClinVar dbSNP |
| 10 | g.102504243C>T | CA377886430 | SUFU | c.91C>T (p.Pro31Ser) c.8+1257C>T (n.8+1257C>T) | ClinVar dbSNP gnomAD v4 |
| 10 | g.102504247del | CA2580081193 | SUFU | c.95del (p.Pro32ArgfsTer?) c.8+1261del (n.8+1261del) | ClinVar |
| 10 | g.102504244C>A | CA377886434 | SUFU | c.92C>A (p.Pro31His) c.8+1258C>A (n.8+1258C>A) | |
| 10 | g.102504244C>G | CA377886436 | SUFU | c.92C>G (p.Pro31Arg) c.8+1258C>G (n.8+1258C>G) | |
| 10 | g.102504244C>T | CA377886437 | SUFU | c.92C>T (p.Pro31Leu) c.8+1258C>T (n.8+1258C>T) | ClinVar dbSNP gnomAD v4 |
| 10 | g.102504245C>A | CA471304843 | SUFU | c.93C>A (p.Pro31=) c.-123C>A (n.-123C>A) c.8+1259C>A (n.8+1259C>A) | |
| 10 | g.102504245C>G | CA471304845 | SUFU | c.93C>G (p.Pro31=) c.-123C>G (n.-123C>G) c.8+1259C>G (n.8+1259C>G) | gnomAD v4 |
| 10 | g.102504245C>T | CA471304844 | SUFU | c.93C>T (p.Pro31=) c.-123C>T (n.-123C>T) c.8+1259C>T (n.8+1259C>T) | |
| 10 | g.102504246C>A | CA377886439 | SUFU | c.94C>A (p.Pro32Thr) c.-122C>A (n.-122C>A) c.8+1260C>A (n.8+1260C>A) | |
| 10 | g.102504246C>G | CA377886441 | SUFU | c.94C>G (p.Pro32Ala) c.-122C>G (n.-122C>G) c.8+1260C>G (n.8+1260C>G) | dbSNP |
| 10 | g.102504246C>T | CA377886443 | SUFU | c.94C>T (p.Pro32Ser) c.-122C>T (n.-122C>T) c.8+1260C>T (n.8+1260C>T) | COSMIC |
| 10 | g.102504247C>A | CA377886444 | SUFU | c.95C>A (p.Pro32Gln) c.-121C>A (n.-121C>A) c.8+1261C>A (n.8+1261C>A) | dbSNP |
| 10 | g.102504247C>G | CA377886446 | SUFU | c.95C>G (p.Pro32Arg) c.-121C>G (n.-121C>G) c.8+1261C>G (n.8+1261C>G) | dbSNP |
| 10 | g.102504247C>T | CA377886448 | SUFU | c.95C>T (p.Pro32Leu) c.-121C>T (n.-121C>T) c.8+1261C>T (n.8+1261C>T) | ClinVar dbSNP |
| 10 | g.102504248G>A | CA471304846 | SUFU | c.96G>A (p.Pro32=) c.-120G>A (n.-120G>A) c.8+1262G>A (n.8+1262G>A) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.102504248G>C | CA471304847 | SUFU | c.96G>C (p.Pro32=) c.-120G>C (n.-120G>C) c.8+1262G>C (n.8+1262G>C) | ClinVar dbSNP gnomAD v2 |
| 10 | g.102504248G= | CA1932719448 | SUFU | c.96G= (p.Pro32=) c.-120G= (n.-120G=) c.8+1262G= (n.8+1262G=) | |
| 10 | g.102504248G>T | CA471304848 | SUFU | c.96G>T (p.Pro32=) c.-120G>T (n.-120G>T) c.8+1262G>T (n.8+1262G>T) | dbSNP COSMIC |
| 10 | g.102504249G>A | CA377886450 | SUFU | c.97G>A (p.Gly33Arg) c.-119G>A (n.-119G>A) c.8+1263G>A (n.8+1263G>A) | |
| 10 | g.102504249G>C | CA377886451 | SUFU | c.97G>C (p.Gly33Arg) c.-119G>C (n.-119G>C) c.8+1263G>C (n.8+1263G>C) | dbSNP |
| 10 | g.102504249G>T | CA377886453 | SUFU | c.97G>T (p.Gly33Ter) c.-119G>T (n.-119G>T) c.8+1263G>T (n.8+1263G>T) | |
| 10 | g.102504250G>A | CA377886454 | SUFU | c.98G>A (p.Gly33Glu) c.-118G>A (n.-118G>A) c.8+1264G>A (n.8+1264G>A) | |
| 10 | g.102504250G>C | CA377886458 | SUFU | c.98G>C (p.Gly33Ala) c.-118G>C (n.-118G>C) c.8+1264G>C (n.8+1264G>C) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 10 | g.102504250G= | CA1932719459 | SUFU | c.98G= (p.Gly33=) c.-118G= (n.-118G=) c.8+1264G= (n.8+1264G=) | |
| 10 | g.102504250G>T | CA377886456 | SUFU | c.98G>T (p.Gly33Val) c.-118G>T (n.-118G>T) c.8+1264G>T (n.8+1264G>T) | |
| 10 | g.102504251A>C | CA471304849 | SUFU | c.99A>C (p.Gly33=) c.-117A>C (n.-117A>C) c.8+1265A>C (n.8+1265A>C) | dbSNP gnomAD v4 |
| 10 | g.102504251A>G | CA471304851 | SUFU | c.99A>G (p.Gly33=) c.-117A>G (n.-117A>G) c.8+1265A>G (n.8+1265A>G) | dbSNP |
| 10 | g.102504251A>T | CA471304850 | SUFU | c.99A>T (p.Gly33=) c.-117A>T (n.-117A>T) c.8+1265A>T (n.8+1265A>T) | |
| 10 | g.102504252C>A | CA377886460 | SUFU | c.100C>A (p.Leu34Met) c.-116C>A (n.-116C>A) c.8+1266C>A (n.8+1266C>A) | |
| 10 | g.102504252C>G | CA377886462 | SUFU | c.100C>G (p.Leu34Val) c.-116C>G (n.-116C>G) c.8+1266C>G (n.8+1266C>G) | |
| 10 | g.102504252C>T | CA471304852 | SUFU | c.100C>T (p.Leu34=) c.-116C>T (n.-116C>T) c.8+1266C>T (n.8+1266C>T) | |
| 10 | g.102504253T>A | CA377886464 | SUFU | c.101T>A (p.Leu34Gln) c.-115T>A (n.-115T>A) c.8+1267T>A (n.8+1267T>A) | |
| 10 | g.102504253T>C | CA377886466 | SUFU | c.101T>C (p.Leu34Pro) c.-115T>C (n.-115T>C) c.8+1267T>C (n.8+1267T>C) | |
| 10 | g.102504253T>G | CA377886468 | SUFU | c.101T>G (p.Leu34Arg) c.-115T>G (n.-115T>G) c.8+1267T>G (n.8+1267T>G) | |
| 10 | g.102504254G>A | CA471304853 | SUFU | c.102G>A (p.Leu34=) c.-114G>A (n.-114G>A) c.8+1268G>A (n.8+1268G>A) | ClinVar dbSNP |
| 10 | g.102504254G>C | CA471304854 | SUFU | c.102G>C (p.Leu34=) c.-114G>C (n.-114G>C) c.8+1268G>C (n.8+1268G>C) | dbSNP |
| 10 | g.102504254G>T | CA471304855 | SUFU | c.102G>T (p.Leu34=) c.-114G>T (n.-114G>T) c.8+1268G>T (n.8+1268G>T) | |
| 10 | g.102504255C>A | CA377886470 | SUFU | c.103C>A (p.His35Asn) c.-113C>A (n.-113C>A) c.8+1269C>A (n.8+1269C>A) | |
| 10 | g.102504255C>G | CA377886472 | SUFU | c.103C>G (p.His35Asp) c.-113C>G (n.-113C>G) c.8+1269C>G (n.8+1269C>G) | |
| 10 | g.102504255C>T | CA377886474 | SUFU | c.103C>T (p.His35Tyr) c.-113C>T (n.-113C>T) c.8+1269C>T (n.8+1269C>T) | ClinVar dbSNP gnomAD v4 |
| 10 | g.102504256A= | CA1932719464 | SUFU | c.104A= (p.His35=) c.-112A= (n.-112A=) c.8+1270A= (n.8+1270A=) | |
| 10 | g.102504256A>C | CA377886476 | SUFU | c.104A>C (p.His35Pro) c.-112A>C (n.-112A>C) c.8+1270A>C (n.8+1270A>C) | dbSNP |
| 10 | g.102504256A>G | CA377886478 | SUFU | c.104A>G (p.His35Arg) c.-112A>G (n.-112A>G) c.8+1270A>G (n.8+1270A>G) | ClinVar dbSNP gnomAD v4 |
| 10 | g.102504256A>T | CA377886480 | SUFU | c.104A>T (p.His35Leu) c.-112A>T (n.-112A>T) c.8+1270A>T (n.8+1270A>T) | |
| 10 | g.102504256dup | CA645568114 | SUFU | c.104dup (p.His35GlnfsTer13) c.-112dup (n.-112dup) c.8+1270dup (n.8+1270dup) | COSMIC |
| 10 | g.102504257C>A | CA377886482 | SUFU | c.105C>A (p.His35Gln) c.-111C>A (n.-111C>A) c.8+1271C>A (n.8+1271C>A) | dbSNP |
| 10 | g.102504257C= | CA1932719473 | SUFU | c.105C= (p.His35=) c.-111C= (n.-111C=) c.8+1271C= (n.8+1271C=) | |
| 10 | g.102504257C>G | CA377886484 | SUFU | c.105C>G (p.His35Gln) c.-111C>G (n.-111C>G) c.8+1271C>G (n.8+1271C>G) | dbSNP |
| 10 | g.102504257C>T | CA5667592 | SUFU | c.105C>T (p.His35=) c.-111C>T (n.-111C>T) c.8+1271C>T (n.8+1271C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 10 | g.102504258G>A | CA377886490 | SUFU | c.106G>A (p.Ala36Thr) c.-110G>A (n.-110G>A) c.8+1272G>A (n.8+1272G>A) | ClinVar dbSNP |
| 10 | g.102504258G>C | CA377886486 | SUFU | c.106G>C (p.Ala36Pro) c.-110G>C (n.-110G>C) c.8+1272G>C (n.8+1272G>C) | dbSNP |
| 10 | g.102504258G>T | CA377886488 | SUFU | c.106G>T (p.Ala36Ser) c.-110G>T (n.-110G>T) c.8+1272G>T (n.8+1272G>T) | |
| 10 | g.102504259C>A | CA377886492 | SUFU | c.107C>A (p.Ala36Asp) c.-109C>A (n.-109C>A) c.8+1273C>A (n.8+1273C>A) | |
| 10 | g.102504259C= | CA1932719486 | SUFU | c.107C= (p.Ala36=) c.-109C= (n.-109C=) c.8+1273C= (n.8+1273C=) | |
| 10 | g.102504259C>G | CA377886494 | SUFU | c.107C>G (p.Ala36Gly) c.-109C>G (n.-109C>G) c.8+1273C>G (n.8+1273C>G) | gnomAD v4 |
| 10 | g.102504259C>T | CA5667593 | SUFU | c.107C>T (p.Ala36Val) c.-109C>T (n.-109C>T) c.8+1273C>T (n.8+1273C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.102504260C>A | CA471304857 | SUFU | c.108C>A (p.Ala36=) c.-108C>A (n.-108C>A) c.8+1274C>A (n.8+1274C>A) | |
| 10 | g.102504260C>G | CA471304858 | SUFU | c.108C>G (p.Ala36=) c.-108C>G (n.-108C>G) c.8+1274C>G (n.8+1274C>G) | |
| 10 | g.102504260C>T | CA471304856 | SUFU | c.108C>T (p.Ala36=) c.-108C>T (n.-108C>T) c.8+1274C>T (n.8+1274C>T) | ClinVar |
| 10 | g.102504261A= | CA1932719494 | SUFU | c.109A= (p.Ile37=) c.-107A= (n.-107A=) c.8+1275A= (n.8+1275A=) | |
| 10 | g.102504261A>C | CA377886497 | SUFU | c.109A>C (p.Ile37Leu) c.-107A>C (n.-107A>C) c.8+1275A>C (n.8+1275A>C) | ClinVar dbSNP |
| 10 | g.102504261A>G | CA5667594 | SUFU | c.109A>G (p.Ile37Val) c.-107A>G (n.-107A>G) c.8+1275A>G (n.8+1275A>G) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.102504261A>T | CA377886500 | SUFU | c.109A>T (p.Ile37Phe) c.-107A>T (n.-107A>T) c.8+1275A>T (n.8+1275A>T) | |
| 10 | g.102504262T>A | CA377886501 | SUFU | c.110T>A (p.Ile37Asn) c.-106T>A (n.-106T>A) c.8+1276T>A (n.8+1276T>A) | ClinVar |
| 10 | g.102504262T>C | CA377886503 | SUFU | c.110T>C (p.Ile37Thr) c.-106T>C (n.-106T>C) c.8+1276T>C (n.8+1276T>C) | |
| 10 | g.102504262T>G | CA377886505 | SUFU | c.110T>G (p.Ile37Ser) c.-106T>G (n.-106T>G) c.8+1276T>G (n.8+1276T>G) | |
| 10 | g.102504262_102504263delinsTC | CA1932719497 | SUFU | c.110_111delinsTC (p.Ile37=) c.-106_-105delinsTC (n.-106_-105delinsTC) c.8+1276_8+1277delinsTC (n.8+1276_8+1277delinsTC) | |
| 10 | g.102504263del | CA279033 | SUFU | c.111del (p.Tyr38ThrfsTer?) c.-105del (n.-105del) c.8+1277del (n.8+1277del) | ClinVar dbSNP |
| 10 | g.102504263C>A | CA471304859 | SUFU | c.111C>A (p.Ile37=) c.-105C>A (n.-105C>A) c.8+1277C>A (n.8+1277C>A) | |
| 10 | g.102504263C>G | CA377886507 | SUFU | c.111C>G (p.Ile37Met) c.-105C>G (n.-105C>G) c.8+1277C>G (n.8+1277C>G) | |
| 10 | g.102504263C>T | CA471304860 | SUFU | c.111C>T (p.Ile37=) c.-105C>T (n.-105C>T) c.8+1277C>T (n.8+1277C>T) | ClinVar |
| 10 | g.102504264T>A | CA377886513 | SUFU | c.112T>A (p.Tyr38Asn) c.-104T>A (n.-104T>A) c.8+1278T>A (n.8+1278T>A) | |
| 10 | g.102504264T>C | CA377886511 | SUFU | c.112T>C (p.Tyr38His) c.-104T>C (n.-104T>C) c.8+1278T>C (n.8+1278T>C) | ClinVar |
| 10 | g.102504264T>G | CA377886510 | SUFU | c.112T>G (p.Tyr38Asp) c.-104T>G (n.-104T>G) c.8+1278T>G (n.8+1278T>G) | |
| 10 | g.102504265A= | CA1932719505 | SUFU | c.113A= (p.Tyr38=) c.-103A= (n.-103A=) c.8+1279A= (n.8+1279A=) | |
| 10 | g.102504265A>C | CA377886515 | SUFU | c.113A>C (p.Tyr38Ser) c.-103A>C (n.-103A>C) c.8+1279A>C (n.8+1279A>C) | dbSNP |
| 10 | g.102504265A>G | CA377886517 | SUFU | c.113A>G (p.Tyr38Cys) c.-103A>G (n.-103A>G) c.8+1279A>G (n.8+1279A>G) | ClinVar dbSNP |
| 10 | g.102504265A>T | CA377886519 | SUFU | c.113A>T (p.Tyr38Phe) c.-103A>T (n.-103A>T) c.8+1279A>T (n.8+1279A>T) | dbSNP |
| 10 | g.102504266C>A | CA377886521 | SUFU | c.114C>A (p.Tyr38Ter) c.-102C>A (n.-102C>A) c.8+1280C>A (n.8+1280C>A) | dbSNP gnomAD v2 |
| 10 | g.102504266C= | CA1932719511 | SUFU | c.114C= (p.Tyr38=) c.-102C= (n.-102C=) c.8+1280C= (n.8+1280C=) | |
| 10 | g.102504266C>G | CA377886522 | SUFU | c.114C>G (p.Tyr38Ter) c.-102C>G (n.-102C>G) c.8+1280C>G (n.8+1280C>G) | |
| 10 | g.102504266C>T | CA471304861 | SUFU | c.114C>T (p.Tyr38=) c.-102C>T (n.-102C>T) c.8+1280C>T (n.8+1280C>T) | ClinVar dbSNP |
| 10 | g.102504267G>A | CA377886524 | SUFU | c.115G>A (p.Gly39Arg) c.-101G>A (n.-101G>A) c.8+1281G>A (n.8+1281G>A) | |
| 10 | g.102504267G>C | CA377886526 | SUFU | c.115G>C (p.Gly39Arg) c.-101G>C (n.-101G>C) c.8+1281G>C (n.8+1281G>C) | dbSNP |
| 10 | g.102504267G>T | CA377886527 | SUFU | c.115G>T (p.Gly39Ter) c.-101G>T (n.-101G>T) c.8+1281G>T (n.8+1281G>T) | |
| 10 | g.102504268G>A | CA377886530 | SUFU | c.116G>A (p.Gly39Glu) c.-100G>A (n.-100G>A) c.8+1282G>A (n.8+1282G>A) | dbSNP gnomAD v2 gnomAD v4 |
| 10 | g.102504268G>C | CA377886532 | SUFU | c.116G>C (p.Gly39Ala) c.-100G>C (n.-100G>C) c.8+1282G>C (n.8+1282G>C) | dbSNP |
| 10 | g.102504268G= | CA1932719516 | SUFU | c.116G= (p.Gly39=) c.-100G= (n.-100G=) c.8+1282G= (n.8+1282G=) | |
| 10 | g.102504268G>T | CA5667595 | SUFU | c.116G>T (p.Gly39Val) c.-100G>T (n.-100G>T) c.8+1282G>T (n.8+1282G>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
| 10 | g.102504269A>C | CA471304862 | SUFU | c.117A>C (p.Gly39=) c.-99A>C (n.-99A>C) c.8+1283A>C (n.8+1283A>C) | |
| 10 | g.102504269A>G | CA471304863 | SUFU | c.117A>G (p.Gly39=) c.-99A>G (n.-99A>G) c.8+1283A>G (n.8+1283A>G) | dbSNP |
| 10 | g.102504269A>T | CA471304864 | SUFU | c.117A>T (p.Gly39=) c.-99A>T (n.-99A>T) c.8+1283A>T (n.8+1283A>T) | |
| 10 | g.102504270G>A | CA377886538 | SUFU | c.118G>A (p.Glu40Lys) c.-98G>A (n.-98G>A) c.8+1284G>A (n.8+1284G>A) | ClinVar dbSNP |
| 10 | g.102504270G>C | CA377886537 | SUFU | c.118G>C (p.Glu40Gln) c.-98G>C (n.-98G>C) c.8+1284G>C (n.8+1284G>C) | |
| 10 | g.102504270G>T | CA377886535 | SUFU | c.118G>T (p.Glu40Ter) c.-98G>T (n.-98G>T) c.8+1284G>T (n.8+1284G>T) | |
| 10 | g.102504271A>C | CA377886539 | SUFU | c.119A>C (p.Glu40Ala) c.-97A>C (n.-97A>C) c.8+1285A>C (n.8+1285A>C) | |
| 10 | g.102504271A>G | CA377886541 | SUFU | c.119A>G (p.Glu40Gly) c.-97A>G (n.-97A>G) c.8+1285A>G (n.8+1285A>G) | ClinVar dbSNP |
| 10 | g.102504271A>T | CA377886543 | SUFU | c.119A>T (p.Glu40Val) c.-97A>T (n.-97A>T) c.8+1285A>T (n.8+1285A>T) | |
| 10 | g.102504272G>A | CA471304865 | SUFU | c.120G>A (p.Glu40=) c.-96G>A (n.-96G>A) c.8+1286G>A (n.8+1286G>A) | ClinVar |
| 10 | g.102504272G>C | CA377886545 | SUFU | c.120G>C (p.Glu40Asp) c.-96G>C (n.-96G>C) c.8+1286G>C (n.8+1286G>C) | |
| 10 | g.102504272G>T | CA377886547 | SUFU | c.120G>T (p.Glu40Asp) c.-96G>T (n.-96G>T) c.8+1286G>T (n.8+1286G>T) | ClinVar |
| 10 | g.102504273T>A | CA377886549 | SUFU | c.121T>A (p.Cys41Ser) c.-95T>A (n.-95T>A) c.8+1287T>A (n.8+1287T>A) | dbSNP |
| 10 | g.102504273T>C | CA377886551 | SUFU | c.121T>C (p.Cys41Arg) c.-95T>C (n.-95T>C) c.8+1287T>C (n.8+1287T>C) | |
| 10 | g.102504273T>G | CA377886553 | SUFU | c.121T>G (p.Cys41Gly) c.-95T>G (n.-95T>G) c.8+1287T>G (n.8+1287T>G) | |
| 10 | g.102504274G>A | CA377886555 | SUFU | c.122G>A (p.Cys41Tyr) c.-94G>A (n.-94G>A) c.8+1288G>A (n.8+1288G>A) | dbSNP |
| 10 | g.102504274G>C | CA377886557 | SUFU | c.122G>C (p.Cys41Ser) c.-94G>C (n.-94G>C) c.8+1288G>C (n.8+1288G>C) | dbSNP |
| 10 | g.102504274G= | CA1932719519 | SUFU | c.122G= (p.Cys41=) c.-94G= (n.-94G=) c.8+1288G= (n.8+1288G=) | |
| 10 | g.102504274G>T | CA377886559 | SUFU | c.122G>T (p.Cys41Phe) c.-94G>T (n.-94G>T) c.8+1288G>T (n.8+1288G>T) | |
| 10 | g.102504280_102504282del | CA2610694436 | SUFU | c.128_130del (p.Arg43del) c.-88_-86del (n.-88_-86del) c.8+1294_8+1296del (n.8+1294_8+1296del) | gnomAD v4 |
| 10 | g.102504275C>A | CA377886561 | SUFU | c.123C>A (p.Cys41Ter) c.-93C>A (n.-93C>A) c.8+1289C>A (n.8+1289C>A) | |
| 10 | g.102504275C= | CA1932719526 | SUFU | c.123C= (p.Cys41=) c.-93C= (n.-93C=) c.8+1289C= (n.8+1289C=) | |
| 10 | g.102504275C>G | CA377886563 | SUFU | c.123C>G (p.Cys41Trp) c.-93C>G (n.-93C>G) c.8+1289C>G (n.8+1289C>G) | |
| 10 | g.102504275C>T | CA471304866 | SUFU | c.123C>T (p.Cys41=) c.-93C>T (n.-93C>T) c.8+1289C>T (n.8+1289C>T) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 10 | g.102504276dup | CA916081614 | SUFU | c.124dup (p.Arg42ProfsTer6) c.-92dup (n.-92dup) c.8+1290dup (n.8+1290dup) | ClinVar dbSNP |
| 10 | g.102504276C>A | CA377886567 | SUFU | c.124C>A (p.Arg42Ser) c.-92C>A (n.-92C>A) c.8+1290C>A (n.8+1290C>A) | gnomAD v4 |
| 10 | g.102504276C= | CA1932719531 | SUFU | c.124C= (p.Arg42=) c.-92C= (n.-92C=) c.8+1290C= (n.8+1290C=) | |
| 10 | g.102504276C>G | CA377886568 | SUFU | c.124C>G (p.Arg42Gly) c.-92C>G (n.-92C>G) c.8+1290C>G (n.8+1290C>G) | |
| 10 | g.102504276C>T | CA377886566 | SUFU | c.124C>T (p.Arg42Cys) c.-92C>T (n.-92C>T) c.8+1290C>T (n.8+1290C>T) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 10 | g.102504277G>A | CA377886571 | SUFU | c.125G>A (p.Arg42His) c.-91G>A (n.-91G>A) c.8+1291G>A (n.8+1291G>A) | dbSNP |
| 10 | g.102504277G>C | CA377886569 | SUFU | c.125G>C (p.Arg42Pro) c.-91G>C (n.-91G>C) c.8+1291G>C (n.8+1291G>C) | dbSNP |
| 10 | g.102504277G= | CA1932719534 | SUFU | c.125G= (p.Arg42=) c.-91G= (n.-91G=) c.8+1291G= (n.8+1291G=) | |
| 10 | g.102504277G>T | CA377886570 | SUFU | c.125G>T (p.Arg42Leu) c.-91G>T (n.-91G>T) c.8+1291G>T (n.8+1291G>T) | dbSNP |
| 10 | g.102504278C>A | CA471304867 | SUFU | c.126C>A (p.Arg42=) c.-90C>A (n.-90C>A) c.8+1292C>A (n.8+1292C>A) | |
| 10 | g.102504278C= | CA1932719538 | SUFU | c.126C= (p.Arg42=) c.-90C= (n.-90C=) c.8+1292C= (n.8+1292C=) | |
| 10 | g.102504278C>G | CA5667596 | SUFU | c.126C>G (p.Arg42=) c.-90C>G (n.-90C>G) c.8+1292C>G (n.8+1292C>G) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.102504278C>T | CA471304868 | SUFU | c.126C>T (p.Arg42=) c.-90C>T (n.-90C>T) c.8+1292C>T (n.8+1292C>T) | |
| 10 | g.102504279C>A | CA377886572 | SUFU | c.127C>A (p.Arg43Ser) c.-89C>A (n.-89C>A) c.8+1293C>A (n.8+1293C>A) | |
| 10 | g.102504279C= | CA1932719546 | SUFU | c.127C= (p.Arg43=) c.-89C= (n.-89C=) c.8+1293C= (n.8+1293C=) | |
| 10 | g.102504279C>G | CA377886573 | SUFU | c.127C>G (p.Arg43Gly) c.-89C>G (n.-89C>G) c.8+1293C>G (n.8+1293C>G) | |
| 10 | g.102504279C>T | CA5667597 | SUFU | c.127C>T (p.Arg43Cys) c.-89C>T (n.-89C>T) c.8+1293C>T (n.8+1293C>T) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 10 | g.102504280G>A | CA377886576 | SUFU | c.128G>A (p.Arg43His) c.-88G>A (n.-88G>A) c.8+1294G>A (n.8+1294G>A) | |
| 10 | g.102504280G>C | CA377886575 | SUFU | c.128G>C (p.Arg43Pro) c.-88G>C (n.-88G>C) c.8+1294G>C (n.8+1294G>C) | dbSNP |
| 10 | g.102504280G>T | CA377886574 | SUFU | c.128G>T (p.Arg43Leu) c.-88G>T (n.-88G>T) c.8+1294G>T (n.8+1294G>T) | |
| 10 | g.102504281C>A | CA471304872 | SUFU | c.129C>A (p.Arg43=) c.-87C>A (n.-87C>A) c.8+1295C>A (n.8+1295C>A) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 10 | g.102504281C= | CA1932719552 | SUFU | c.129C= (p.Arg43=) c.-87C= (n.-87C=) c.8+1295C= (n.8+1295C=) | |
| 10 | g.102504281C>G | CA471304869 | SUFU | c.129C>G (p.Arg43=) c.-87C>G (n.-87C>G) c.8+1295C>G (n.8+1295C>G) | ClinVar dbSNP |
| 10 | g.102504281C>T | CA471304870 | SUFU | c.129C>T (p.Arg43=) c.-87C>T (n.-87C>T) c.8+1295C>T (n.8+1295C>T) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 10 | g.102504282C>A | CA377886577 | SUFU | c.130C>A (p.Leu44Ile) c.-86C>A (n.-86C>A) c.8+1296C>A (n.8+1296C>A) | |
| 10 | g.102504282C= | CA1932719556 | SUFU | c.130C= (p.Leu44=) c.-86C= (n.-86C=) c.8+1296C= (n.8+1296C=) | |
| 10 | g.102504282C>G | CA377886578 | SUFU | c.130C>G (p.Leu44Val) c.-86C>G (n.-86C>G) c.8+1296C>G (n.8+1296C>G) | gnomAD v4 |
| 10 | g.102504282C>T | CA377886579 | SUFU | c.130C>T (p.Leu44Phe) c.-86C>T (n.-86C>T) c.8+1296C>T (n.8+1296C>T) | ClinVar dbSNP gnomAD v4 |
| 10 | g.102504283T>A | CA377886580 | SUFU | c.131T>A (p.Leu44His) c.-85T>A (n.-85T>A) c.8+1297T>A (n.8+1297T>A) | |
| 10 | g.102504283T>C | CA5667598 | SUFU | c.131T>C (p.Leu44Pro) c.-85T>C (n.-85T>C) c.8+1297T>C (n.8+1297T>C) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 10 | g.102504283T>G | CA377886581 | SUFU | c.131T>G (p.Leu44Arg) c.-85T>G (n.-85T>G) c.8+1297T>G (n.8+1297T>G) | |
| 10 | g.102504283T= | CA1932719561 | SUFU | c.131T= (p.Leu44=) c.-85T= (n.-85T=) c.8+1297T= (n.8+1297T=) | |
| 10 | g.102504284_102504285del | CA2610694437 | SUFU | c.132_133del (p.Tyr45ProfsTer2) c.-84_-83del (n.-84_-83del) c.8+1298_8+1299del (n.8+1298_8+1299del) | gnomAD v4 |
| 10 | g.102504284T>A | CA471304875 | SUFU | c.132T>A (p.Leu44=) c.-84T>A (n.-84T>A) c.8+1298T>A (n.8+1298T>A) | |
| 10 | g.102504284T>C | CA471304876 | SUFU | c.132T>C (p.Leu44=) c.-84T>C (n.-84T>C) c.8+1298T>C (n.8+1298T>C) | |
| 10 | g.102504284T>G | CA471304877 | SUFU | c.132T>G (p.Leu44=) c.-84T>G (n.-84T>G) c.8+1298T>G (n.8+1298T>G) | ClinVar |
| 10 | g.102504285T>A | CA377886582 | SUFU | c.133T>A (p.Tyr45Asn) c.-83T>A (n.-83T>A) c.8+1299T>A (n.8+1299T>A) | |
| 10 | g.102504285T>C | CA377886584 | SUFU | c.133T>C (p.Tyr45His) c.-83T>C (n.-83T>C) c.8+1299T>C (n.8+1299T>C) | |
| 10 | g.102504285T>G | CA377886583 | SUFU | c.133T>G (p.Tyr45Asp) c.-83T>G (n.-83T>G) c.8+1299T>G (n.8+1299T>G) | |
| 10 | g.102504286A= | CA1932719568 | SUFU | c.134A= (p.Tyr45=) c.-82A= (n.-82A=) c.8+1300A= (n.8+1300A=) | |
| 10 | g.102504286A>C | CA5667599 | SUFU | c.134A>C (p.Tyr45Ser) c.-82A>C (n.-82A>C) c.8+1300A>C (n.8+1300A>C) | dbSNP ExAC gnomAD v4 |
| 10 | g.102504286A>G | CA377886585 | SUFU | c.134A>G (p.Tyr45Cys) c.-82A>G (n.-82A>G) c.8+1300A>G (n.8+1300A>G) | |
| 10 | g.102504286A>T | CA377886586 | SUFU | c.134A>T (p.Tyr45Phe) c.-82A>T (n.-82A>T) c.8+1300A>T (n.8+1300A>T) | ClinVar dbSNP |
| 10 | g.102504287C>A | CA377886587 | SUFU | c.135C>A (p.Tyr45Ter) c.-81C>A (n.-81C>A) c.8+1301C>A (n.8+1301C>A) | |
| 10 | g.102504287C= | CA1932719576 | SUFU | c.135C= (p.Tyr45=) c.-81C= (n.-81C=) c.8+1301C= (n.8+1301C=) | |
| 10 | g.102504287C>G | CA377886588 | SUFU | c.135C>G (p.Tyr45Ter) c.-81C>G (n.-81C>G) c.8+1301C>G (n.8+1301C>G) | |
| 10 | g.102504287C>T | CA471304879 | SUFU | c.135C>T (p.Tyr45=) c.-81C>T (n.-81C>T) c.8+1301C>T (n.8+1301C>T) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 10 | g.102504288C>A | CA377886590 | SUFU | c.136C>A (p.Pro46Thr) c.-80C>A (n.-80C>A) c.8+1302C>A (n.8+1302C>A) | ClinVar |
| 10 | g.102504288C= | CA1932719579 | SUFU | c.136C= (p.Pro46=) c.-80C= (n.-80C=) c.8+1302C= (n.8+1302C=) | |
| 10 | g.102504288C>G | CA377886592 | SUFU | c.136C>G (p.Pro46Ala) c.-80C>G (n.-80C>G) c.8+1302C>G (n.8+1302C>G) | gnomAD v4 |
| 10 | g.102504288C>T | CA5667600 | SUFU | c.136C>T (p.Pro46Ser) c.-80C>T (n.-80C>T) c.8+1302C>T (n.8+1302C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 10 | g.102504289C>A | CA377886595 | SUFU | c.137C>A (p.Pro46His) c.-79C>A (n.-79C>A) c.8+1303C>A (n.8+1303C>A) | |
| 10 | g.102504289C>G | CA377886597 | SUFU | c.137C>G (p.Pro46Arg) c.-79C>G (n.-79C>G) c.8+1303C>G (n.8+1303C>G) | ClinVar |
| 10 | g.102504289C>T | CA377886599 | SUFU | c.137C>T (p.Pro46Leu) c.-79C>T (n.-79C>T) c.8+1303C>T (n.8+1303C>T) | ClinVar dbSNP gnomAD v4 |
| 10 | g.102504290_102504293del | CA2580081197 | SUFU | c.138_141del (p.Asp47SerfsTer?) c.-78_-75del (n.-78_-75del) c.8+1304_8+1307del (n.8+1304_8+1307del) | ClinVar |
| 10 | g.102504290T>A | CA471304880 | SUFU | c.138T>A (p.Pro46=) c.-78T>A (n.-78T>A) c.8+1304T>A (n.8+1304T>A) | ClinVar |
| 10 | g.102504290T>C | CA471304881 | SUFU | c.138T>C (p.Pro46=) c.-78T>C (n.-78T>C) c.8+1304T>C (n.8+1304T>C) | ClinVar |
| 10 | g.102504290T>G | CA471304882 | SUFU | c.138T>G (p.Pro46=) c.-78T>G (n.-78T>G) c.8+1304T>G (n.8+1304T>G) | ClinVar |