Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.48703362G>A | CA406710205 | FUT2 | c.406G>A (p.Glu136Lys) n.487C>T | |
19 | g.48703362G>C | CA406710204 | FUT2 | c.406G>C (p.Glu136Gln) n.487C>G | |
19 | g.48703362G>T | CA406710202 | FUT2 | c.406G>T (p.Glu136Ter) n.487C>A | |
19 | g.48703362_48703364delinsGAA | CA2340029989 | FUT2 | c.406_408delinsGAA (p.Glu136=) n.485_487delinsTTC | |
19 | g.48703363A>C | CA406710207 | FUT2 | c.407A>C (p.Glu136Ala) n.486T>G | |
19 | g.48703363A>G | CA406710208 | FUT2 | c.407A>G (p.Glu136Gly) n.486T>C | |
19 | g.48703363A>T | CA406710209 | FUT2 | c.407A>T (p.Glu136Val) n.486T>A | |
19 | g.48703363_48703364del | CA2340029990 | FUT2 | c.407_408del (p.Glu136ValfsTer?) n.485_486del | dbSNP |
19 | g.48703364A= | CA2340029991 | FUT2 | c.408A= (p.Glu136=) n.485T= | |
19 | g.48703364A>C | CA406710212 | FUT2 | c.408A>C (p.Glu136Asp) n.485T>G | |
19 | g.48703364A>G | CA9556234 | FUT2 | c.408A>G (p.Glu136=) n.485T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703364A>T | CA406710215 | FUT2 | c.408A>T (p.Glu136Asp) n.485T>A | |
19 | g.48703365del | CA645614262 | FUT2 | c.409del (p.Tyr137ThrfsTer?) n.484del | COSMIC |
19 | g.48703365T>A | CA406710218 | FUT2 | c.409T>A (p.Tyr137Asn) n.484A>T | |
19 | g.48703365T>C | CA406710220 | FUT2 | c.409T>C (p.Tyr137His) n.484A>G | |
19 | g.48703365T>G | CA406710222 | FUT2 | c.409T>G (p.Tyr137Asp) n.484A>C | |
19 | g.48703366A= | CA2340029992 | FUT2 | c.410A= (p.Tyr137=) n.483T= | |
19 | g.48703366A>C | CA406710225 | FUT2 | c.410A>C (p.Tyr137Ser) n.483T>G | dbSNP gnomAD v4 |
19 | g.48703366A>G | CA406710226 | FUT2 | c.410A>G (p.Tyr137Cys) n.483T>C | |
19 | g.48703366A>T | CA406710229 | FUT2 | c.410A>T (p.Tyr137Phe) n.483T>A | |
19 | g.48703366_48703367insACCC | CA309352413 | FUT2 | c.410_411insACCC (p.Tyr137Ter) n.482_483insGGGT | dbSNP |
19 | g.48703367C>A | CA406710233 | FUT2 | c.411C>A (p.Tyr137Ter) n.482G>T | |
19 | g.48703367C>G | CA406710232 | FUT2 | c.411C>G (p.Tyr137Ter) n.482G>C | |
19 | g.48703367C>T | CA508272338 | FUT2 | c.411C>T (p.Tyr137=) n.482G>A | gnomAD v4 |
19 | g.48703368C>A | CA406710236 | FUT2 | c.412C>A (p.Arg138Ser) n.481G>T | |
19 | g.48703368C= | CA2340029993 | FUT2 | c.412C= (p.Arg138=) n.481G= | |
19 | g.48703368C>G | CA406710239 | FUT2 | c.412C>G (p.Arg138Gly) n.481G>C | |
19 | g.48703368C>T | CA9556235 | FUT2 | c.412C>T (p.Arg138Cys) n.481G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703369G>A | CA9556236 | FUT2 | c.413G>A (p.Arg138His) n.480C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.48703369G>C | CA406710242 | FUT2 | c.413G>C (p.Arg138Pro) n.480C>G | COSMIC |
19 | g.48703369G= | CA2340029994 | FUT2 | c.413G= (p.Arg138=) n.480C= | |
19 | g.48703369G>T | CA406710244 | FUT2 | c.413G>T (p.Arg138Leu) n.480C>A | |
19 | g.48703370C>A | CA508272341 | FUT2 | c.414C>A (p.Arg138=) n.479G>T | |
19 | g.48703370C= | CA2340029995 | FUT2 | c.414C= (p.Arg138=) n.479G= | |
19 | g.48703370C>G | CA508272343 | FUT2 | c.414C>G (p.Arg138=) n.479G>C | |
19 | g.48703370C>T | CA9556237 | FUT2 | c.414C>T (p.Arg138=) n.479G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703371C>A | CA406710250 | FUT2 | c.415C>A (p.His139Asn) n.478G>T | |
19 | g.48703371C>G | CA406710252 | FUT2 | c.415C>G (p.His139Asp) n.478G>C | |
19 | g.48703371C>T | CA406710254 | FUT2 | c.415C>T (p.His139Tyr) n.478G>A | gnomAD v4 |
19 | g.48703372A>C | CA406710256 | FUT2 | c.416A>C (p.His139Pro) n.477T>G | |
19 | g.48703372A>G | CA406710258 | FUT2 | c.416A>G (p.His139Arg) n.477T>C | |
19 | g.48703372A>T | CA406710260 | FUT2 | c.416A>T (p.His139Leu) n.477T>A | |
19 | g.48703373C>A | CA406710263 | FUT2 | c.417C>A (p.His139Gln) n.476G>T | |
19 | g.48703373C= | CA2340029996 | FUT2 | c.417C= (p.His139=) n.476G= | |
19 | g.48703373C>G | CA406710264 | FUT2 | c.417C>G (p.His139Gln) n.476G>C | dbSNP |
19 | g.48703373C>T | CA508272350 | FUT2 | c.417C>T (p.His139=) n.476G>A | |
19 | g.48703374A= | CA2340029997 | FUT2 | c.418A= (p.Ile140=) n.475T= | |
19 | g.48703374A>C | CA406710268 | FUT2 | c.418A>C (p.Ile140Leu) n.475T>G | dbSNP |
19 | g.48703374A>G | CA406710271 | FUT2 | c.418A>G (p.Ile140Val) n.475T>C | |
19 | g.48703374A>T | CA122800 | FUT2 | c.418A>T (p.Ile140Phe) n.475T>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703375T>A | CA406710274 | FUT2 | c.419T>A (p.Ile140Asn) n.474A>T | dbSNP |
19 | g.48703375T>C | CA406710276 | FUT2 | c.419T>C (p.Ile140Thr) n.474A>G | |
19 | g.48703375T>G | CA406710277 | FUT2 | c.419T>G (p.Ile140Ser) n.474A>C | |
19 | g.48703375T= | CA2340029998 | FUT2 | c.419T= (p.Ile140=) n.474A= | |
19 | g.48703376C>A | CA508272354 | FUT2 | c.420C>A (p.Ile140=) n.473G>T | |
19 | g.48703376C= | CA2340029999 | FUT2 | c.420C= (p.Ile140=) n.473G= | |
19 | g.48703376C>G | CA406710280 | FUT2 | c.420C>G (p.Ile140Met) n.473G>C | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703376C>T | CA508272353 | FUT2 | c.420C>T (p.Ile140=) n.473G>A | dbSNP gnomAD v3 gnomAD v4 |
19 | g.48703377C>A | CA406710283 | FUT2 | c.421C>A (p.Pro141Thr) n.472G>T | gnomAD v4 |
19 | g.48703377C>G | CA406710285 | FUT2 | c.421C>G (p.Pro141Ala) n.472G>C | |
19 | g.48703377C>T | CA406710287 | FUT2 | c.421C>T (p.Pro141Ser) n.472G>A | |
19 | g.48703378C>A | CA406710290 | FUT2 | c.422C>A (p.Pro141Gln) n.471G>T | gnomAD v4 |
19 | g.48703378C= | CA2340030000 | FUT2 | c.422C= (p.Pro141=) n.471G= | |
19 | g.48703378C>G | CA9556238 | FUT2 | c.422C>G (p.Pro141Arg) n.471G>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.48703378C>T | CA9556239 | FUT2 | c.422C>T (p.Pro141Leu) n.471G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703379G>A | CA9556241 | FUT2 | c.423G>A (p.Pro141=) n.470C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
19 | g.48703379G>C | CA9556242 | FUT2 | c.423G>C (p.Pro141=) n.470C>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.48703379G= | CA2340030001 | FUT2 | c.423G= (p.Pro141=) n.470C= | |
19 | g.48703379G>T | CA9556240 | FUT2 | c.423G>T (p.Pro141=) n.470C>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703383dup | CA2340030002 | FUT2 | c.427dup (p.Glu143GlyfsTer?) n.470dup | dbSNP |
19 | g.48703383del | CA645614263 | FUT2 | c.427del (p.Glu143SerfsTer?) n.470del | COSMIC |
19 | g.48703380G>A | CA406710302 | FUT2 | c.424G>A (p.Gly142Arg) n.469C>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703380G>C | CA406710304 | FUT2 | c.424G>C (p.Gly142Arg) n.469C>G | gnomAD v4 |
19 | g.48703380G= | CA2340030003 | FUT2 | c.424G= (p.Gly142=) n.469C= | |
19 | g.48703380G>T | CA406710306 | FUT2 | c.424G>T (p.Gly142Trp) n.469C>A | |
19 | g.48703381G>A | CA406710307 | FUT2 | c.425G>A (p.Gly142Glu) n.468C>T | COSMIC |
19 | g.48703381G>C | CA406710309 | FUT2 | c.425G>C (p.Gly142Ala) n.468C>G | dbSNP gnomAD v2 |
19 | g.48703381G= | CA2340030004 | FUT2 | c.425G= (p.Gly142=) n.468C= | |
19 | g.48703381G>T | CA406710310 | FUT2 | c.425G>T (p.Gly142Val) n.468C>A | |
19 | g.48703382G>A | CA508272367 | FUT2 | c.426G>A (p.Gly142=) n.467C>T | gnomAD v4 |
19 | g.48703382G>C | CA508272368 | FUT2 | c.426G>C (p.Gly142=) n.467C>G | |
19 | g.48703382G>T | CA508272369 | FUT2 | c.426G>T (p.Gly142=) n.467C>A | |
19 | g.48703382_48703383insC | CA2586240159 | FUT2 | c.426_427insC (p.Glu143ArgfsTer?) n.466_467insG | gnomAD v4 |
19 | g.48703382_48703383insCGCT | CA2586240157 | FUT2 | c.426_427insCGCT (p.Glu143ArgfsTer2) n.466_467insAGCG | gnomAD v4 |
19 | g.48703382_48703383insCGCTGT | CA2586240158 | FUT2 | c.426_427insCGCTGT (p.Gly142_Glu143insArgCys) n.466_467insACAGCG | gnomAD v4 |
19 | g.48703383G>A | CA406710311 | FUT2 | c.427G>A (p.Glu143Lys) n.466C>T | |
19 | g.48703383G>C | CA406710313 | FUT2 | c.427G>C (p.Glu143Gln) n.466C>G | gnomAD v4 |
19 | g.48703383G= | CA2340030005 | FUT2 | c.427G= (p.Glu143=) n.466C= | |
19 | g.48703383G>T | CA406710314 | FUT2 | c.427G>T (p.Glu143Ter) n.466C>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703383_48703384insC | CA2340030006 | FUT2 | c.427_428insC (p.Glu143AlafsTer?) n.465_466insG | dbSNP gnomAD v4 |
19 | g.48703384A= | CA2340030007 | FUT2 | c.428A= (p.Glu143=) n.465T= | |
19 | g.48703384A>C | CA406710316 | FUT2 | c.428A>C (p.Glu143Ala) n.465T>G | |
19 | g.48703384A>G | CA406710318 | FUT2 | c.428A>G (p.Glu143Gly) n.465T>C | |
19 | g.48703384A>T | CA406710320 | FUT2 | c.428A>T (p.Glu143Val) n.465T>A | dbSNP gnomAD v4 |
19 | g.48703385G>A | CA9556243 | FUT2 | c.429G>A (p.Glu143=) n.464C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703385G>C | CA406710324 | FUT2 | c.429G>C (p.Glu143Asp) n.464C>G | |
19 | g.48703385G= | CA2340030008 | FUT2 | c.429G= (p.Glu143=) n.464C= | |
19 | g.48703385G>T | CA406710322 | FUT2 | c.429G>T (p.Glu143Asp) n.464C>A | |
19 | g.48703386T>A | CA406710327 | FUT2 | c.430T>A (p.Tyr144Asn) n.463A>T | |
19 | g.48703386T>C | CA406710329 | FUT2 | c.430T>C (p.Tyr144His) n.463A>G | |
19 | g.48703386T>G | CA406710330 | FUT2 | c.430T>G (p.Tyr144Asp) n.463A>C | dbSNP gnomAD v3 gnomAD v4 |
19 | g.48703386T= | CA2340030009 | FUT2 | c.430T= (p.Tyr144=) n.463A= | |
19 | g.48703386_48703388delinsTAC | CA2340030010 | FUT2 | c.430_432delinsTAC (p.Tyr144=) n.461_463delinsGTA | |
19 | g.48703387A>C | CA406710333 | FUT2 | c.431A>C (p.Tyr144Ser) n.462T>G | |
19 | g.48703387A>G | CA406710335 | FUT2 | c.431A>G (p.Tyr144Cys) n.462T>C | |
19 | g.48703387A>T | CA406710337 | FUT2 | c.431A>T (p.Tyr144Phe) n.462T>A | ClinVar |
19 | g.48703387_48703388del | CA2340030011 | FUT2 | c.431_432del (p.Tyr144CysfsTer?) n.461_462del | dbSNP gnomAD v4 |
19 | g.48703388C>A | CA406710342 | FUT2 | c.432C>A (p.Tyr144Ter) n.461G>T | |
19 | g.48703388C= | CA2340030012 | FUT2 | c.432C= (p.Tyr144=) n.461G= | |
19 | g.48703388C>G | CA406710340 | FUT2 | c.432C>G (p.Tyr144Ter) n.461G>C | |
19 | g.48703388C>T | CA508272379 | FUT2 | c.432C>T (p.Tyr144=) n.461G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703389G>A | CA9556244 | FUT2 | c.433G>A (p.Val145Ile) n.460C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
19 | g.48703389G>C | CA406710349 | FUT2 | c.433G>C (p.Val145Leu) n.460C>G | |
19 | g.48703389G= | CA2340030013 | FUT2 | c.433G= (p.Val145=) n.460C= | |
19 | g.48703389G>T | CA406710351 | FUT2 | c.433G>T (p.Val145Phe) n.460C>A | |
19 | g.48703390T>A | CA406710355 | FUT2 | c.434T>A (p.Val145Asp) n.459A>T | |
19 | g.48703390T>C | CA406710356 | FUT2 | c.434T>C (p.Val145Ala) n.459A>G | dbSNP gnomAD v4 |
19 | g.48703390T>G | CA406710358 | FUT2 | c.434T>G (p.Val145Gly) n.459A>C | gnomAD v3 gnomAD v4 |
19 | g.48703390T= | CA2340030014 | FUT2 | c.434T= (p.Val145=) n.459A= | |
19 | g.48703391C>A | CA508272382 | FUT2 | c.435C>A (p.Val145=) n.458G>T | |
19 | g.48703391C>G | CA508272383 | FUT2 | c.435C>G (p.Val145=) n.458G>C | |
19 | g.48703391C>T | CA508272384 | FUT2 | c.435C>T (p.Val145=) n.458G>A | |
19 | g.48703392C>A | CA406710363 | FUT2 | c.436C>A (p.Arg146Ser) n.457G>T | |
19 | g.48703392C= | CA2340030015 | FUT2 | c.436C= (p.Arg146=) n.457G= | |
19 | g.48703392C>G | CA406710362 | FUT2 | c.436C>G (p.Arg146Gly) n.457G>C | |
19 | g.48703392C>T | CA9556245 | FUT2 | c.436C>T (p.Arg146Cys) n.457G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703393G>A | CA9556246 | FUT2 | c.437G>A (p.Arg146His) n.456C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703393G>C | CA406710368 | FUT2 | c.437G>C (p.Arg146Pro) n.456C>G | dbSNP gnomAD v3 gnomAD v4 |
19 | g.48703393G= | CA2340030016 | FUT2 | c.437G= (p.Arg146=) n.456C= | |
19 | g.48703393G>T | CA406710366 | FUT2 | c.437G>T (p.Arg146Leu) n.456C>A | |
19 | g.48703394C>A | CA508272387 | FUT2 | c.438C>A (p.Arg146=) n.455G>T | |
19 | g.48703394C= | CA2340030017 | FUT2 | c.438C= (p.Arg146=) n.455G= | |
19 | g.48703394C>G | CA508272389 | FUT2 | c.438C>G (p.Arg146=) n.455G>C | |
19 | g.48703394C>T | CA309352426 | FUT2 | c.438C>T (p.Arg146=) n.455G>A | dbSNP gnomAD v3 gnomAD v4 |
19 | g.48703395T>A | CA406710371 | FUT2 | c.439T>A (p.Phe147Ile) n.454A>T | |
19 | g.48703395T>C | CA406710375 | FUT2 | c.439T>C (p.Phe147Leu) n.454A>G | dbSNP gnomAD v4 |
19 | g.48703395T>G | CA406710373 | FUT2 | c.439T>G (p.Phe147Val) n.454A>C | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703395T= | CA2340030018 | FUT2 | c.439T= (p.Phe147=) n.454A= | |
19 | g.48703396T>A | CA406710378 | FUT2 | c.440T>A (p.Phe147Tyr) n.453A>T | gnomAD v4 |
19 | g.48703396T>C | CA406710382 | FUT2 | c.440T>C (p.Phe147Ser) n.453A>G | dbSNP |
19 | g.48703396T>G | CA406710380 | FUT2 | c.440T>G (p.Phe147Cys) n.453A>C | |
19 | g.48703396T= | CA2340030019 | FUT2 | c.440T= (p.Phe147=) n.453A= | |
19 | g.48703397C>A | CA406710385 | FUT2 | c.441C>A (p.Phe147Leu) n.452G>T | |
19 | g.48703397C>G | CA406710386 | FUT2 | c.441C>G (p.Phe147Leu) n.452G>C | |
19 | g.48703397C>T | CA508272391 | FUT2 | c.441C>T (p.Phe147=) n.452G>A | |
19 | g.48703398A>C | CA406710389 | FUT2 | c.442A>C (p.Thr148Pro) n.451T>G | |
19 | g.48703398A>G | CA406710393 | FUT2 | c.442A>G (p.Thr148Ala) n.451T>C | |
19 | g.48703398A>T | CA406710391 | FUT2 | c.442A>T (p.Thr148Ser) n.451T>A | |
19 | g.48703399C>A | CA406710396 | FUT2 | c.443C>A (p.Thr148Asn) n.450G>T | |
19 | g.48703399C>G | CA406710399 | FUT2 | c.443C>G (p.Thr148Ser) n.450G>C | |
19 | g.48703399C>T | CA406710397 | FUT2 | c.443C>T (p.Thr148Ile) n.450G>A | |
19 | g.48703400C>A | CA508272397 | FUT2 | c.444C>A (p.Thr148=) n.449G>T | |
19 | g.48703400C= | CA2340030020 | FUT2 | c.444C= (p.Thr148=) n.449G= | |
19 | g.48703400C>G | CA9556247 | FUT2 | c.444C>G (p.Thr148=) n.449G>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
19 | g.48703400C>T | CA9556248 | FUT2 | c.444C>T (p.Thr148=) n.449G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703401G>A | CA9556249 | FUT2 | c.445G>A (p.Gly149Ser) n.448C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
19 | g.48703401G>C | CA406710404 | FUT2 | c.445G>C (p.Gly149Arg) n.448C>G | |
19 | g.48703401G= | CA2340030021 | FUT2 | c.445G= (p.Gly149=) n.448C= | |
19 | g.48703401G>T | CA406710402 | FUT2 | c.445G>T (p.Gly149Cys) n.448C>A | |
19 | g.48703402G>A | CA406710407 | FUT2 | c.446G>A (p.Gly149Asp) n.447C>T | |
19 | g.48703402G>C | CA406710410 | FUT2 | c.446G>C (p.Gly149Ala) n.447C>G | |
19 | g.48703402G>T | CA406710412 | FUT2 | c.446G>T (p.Gly149Val) n.447C>A | |
19 | g.48703403C>A | CA508272403 | FUT2 | c.447C>A (p.Gly149=) n.446G>T | |
19 | g.48703403C>G | CA508272405 | FUT2 | c.447C>G (p.Gly149=) n.446G>C | |
19 | g.48703403C>T | CA508272404 | FUT2 | c.447C>T (p.Gly149=) n.446G>A | |
19 | g.48703404T>A | CA406710416 | FUT2 | c.448T>A (p.Tyr150Asn) n.445A>T | |
19 | g.48703404T>C | CA406710418 | FUT2 | c.448T>C (p.Tyr150His) n.445A>G | |
19 | g.48703404T>G | CA406710420 | FUT2 | c.448T>G (p.Tyr150Asp) n.445A>C | |
19 | g.48703405A>C | CA406710421 | FUT2 | c.449A>C (p.Tyr150Ser) n.444T>G | |
19 | g.48703405A>G | CA406710422 | FUT2 | c.449A>G (p.Tyr150Cys) n.444T>C | |
19 | g.48703405A>T | CA406710424 | FUT2 | c.449A>T (p.Tyr150Phe) n.444T>A | |
19 | g.48703406C>A | CA9556250 | FUT2 | c.450C>A (p.Tyr150Ter) n.443G>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.48703406C= | CA2340030022 | FUT2 | c.450C= (p.Tyr150=) n.443G= | |
19 | g.48703406C>G | CA406710428 | FUT2 | c.450C>G (p.Tyr150Ter) n.443G>C | |
19 | g.48703406C>T | CA508272408 | FUT2 | c.450C>T (p.Tyr150=) n.443G>A | |
19 | g.48703409del | CA2838444151 | FUT2 | c.453del (p.Cys152AlafsTer?) n.443del | |
19 | g.48703407C>A | CA406710430 | FUT2 | c.451C>A (p.Pro151Thr) n.442G>T | gnomAD v3 gnomAD v4 |
19 | g.48703407C= | CA2340030023 | FUT2 | c.451C= (p.Pro151=) n.442G= | |
19 | g.48703407C>G | CA406710432 | FUT2 | c.451C>G (p.Pro151Ala) n.442G>C | |
19 | g.48703407C>T | CA406710434 | FUT2 | c.451C>T (p.Pro151Ser) n.442G>A | dbSNP gnomAD v4 |
19 | g.48703408C>A | CA406710440 | FUT2 | c.452C>A (p.Pro151His) n.441G>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703408C= | CA2340030024 | FUT2 | c.452C= (p.Pro151=) n.441G= | |
19 | g.48703408C>G | CA406710439 | FUT2 | c.452C>G (p.Pro151Arg) n.441G>C | |
19 | g.48703408C>T | CA406710437 | FUT2 | c.452C>T (p.Pro151Leu) n.441G>A | COSMIC |
19 | g.48703409C>A | CA508272537 | FUT2 | c.453C>A (p.Pro151=) n.440G>T | |
19 | g.48703409C>G | CA508272540 | FUT2 | c.453C>G (p.Pro151=) n.440G>C | |
19 | g.48703409C>T | CA508272544 | FUT2 | c.453C>T (p.Pro151=) n.440G>A | gnomAD v4 |
19 | g.48703410T>A | CA406710443 | FUT2 | c.454T>A (p.Cys152Ser) n.439A>T | |
19 | g.48703410T>C | CA406710445 | FUT2 | c.454T>C (p.Cys152Arg) n.439A>G | dbSNP |
19 | g.48703410T>G | CA406710447 | FUT2 | c.454T>G (p.Cys152Gly) n.439A>C | |
19 | g.48703410T= | CA2340030025 | FUT2 | c.454T= (p.Cys152=) n.439A= | |
19 | g.48703411G>A | CA406710450 | FUT2 | c.455G>A (p.Cys152Tyr) n.438C>T | |
19 | g.48703411G>C | CA406710451 | FUT2 | c.455G>C (p.Cys152Ser) n.438C>G | gnomAD v4 |
19 | g.48703411G>T | CA406710453 | FUT2 | c.455G>T (p.Cys152Phe) n.438C>A | |
19 | g.48703412C>A | CA406710456 | FUT2 | c.456C>A (p.Cys152Ter) n.437G>T | |
19 | g.48703412C= | CA2340030026 | FUT2 | c.456C= (p.Cys152=) n.437G= | |
19 | g.48703412C>G | CA406710458 | FUT2 | c.456C>G (p.Cys152Trp) n.437G>C | dbSNP gnomAD v2 |
19 | g.48703412C>T | CA508272550 | FUT2 | c.456C>T (p.Cys152=) n.437G>A | dbSNP gnomAD v2 gnomAD v4 |
19 | g.48703413T>A | CA406710461 | FUT2 | c.457T>A (p.Ser153Thr) n.436A>T | |
19 | g.48703413T>C | CA406710462 | FUT2 | c.457T>C (p.Ser153Pro) n.436A>G | |
19 | g.48703413T>G | CA406710463 | FUT2 | c.457T>G (p.Ser153Ala) n.436A>C | |
19 | g.48703414C>A | CA406710465 | FUT2 | c.458C>A (p.Ser153Tyr) n.435G>T | |
19 | g.48703414C= | CA2340030027 | FUT2 | c.458C= (p.Ser153=) n.435G= | |
19 | g.48703414C>G | CA406710467 | FUT2 | c.458C>G (p.Ser153Cys) n.435G>C | dbSNP |
19 | g.48703414C>T | CA406710468 | FUT2 | c.458C>T (p.Ser153Phe) n.435G>A | gnomAD v4 |
19 | g.48703415C>A | CA508272551 | FUT2 | c.459C>A (p.Ser153=) n.434G>T | |
19 | g.48703415C= | CA2340030028 | FUT2 | c.459C= (p.Ser153=) n.434G= | |
19 | g.48703415C>G | CA508272552 | FUT2 | c.459C>G (p.Ser153=) n.434G>C | dbSNP gnomAD v2 gnomAD v4 |
19 | g.48703415C>T | CA508272553 | FUT2 | c.459C>T (p.Ser153=) n.434G>A | |
19 | g.48703417_48703425del | CA2586240160 | FUT2 | c.461_469del (p.Trp154_Phe156del) n.426_434del | gnomAD v4 |
19 | g.48703416T>A | CA406710473 | FUT2 | c.460T>A (p.Trp154Arg) n.433A>T | |
19 | g.48703416T>C | CA406710474 | FUT2 | c.460T>C (p.Trp154Arg) n.433A>G | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703416T>G | CA406710472 | FUT2 | c.460T>G (p.Trp154Gly) n.433A>C | |
19 | g.48703416T= | CA2340030029 | FUT2 | c.460T= (p.Trp154=) n.433A= | |
19 | g.48703417G>A | CA122797 | FUT2 | c.461G>A (p.Trp154Ter) n.432C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703417G>C | CA406710483 | FUT2 | c.461G>C (p.Trp154Ser) n.432C>G | |
19 | g.48703417G= | CA2340030030 | FUT2 | c.461G= (p.Trp154=) n.432C= | |
19 | g.48703417G>T | CA406710485 | FUT2 | c.461G>T (p.Trp154Leu) n.432C>A | |
19 | g.48703418G>A | CA9556251 | FUT2 | c.462G>A (p.Trp154Ter) n.431C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703418G>C | CA406710488 | FUT2 | c.462G>C (p.Trp154Cys) n.431C>G | |
19 | g.48703418G= | CA2340030031 | FUT2 | c.462G= (p.Trp154=) n.431C= | |
19 | g.48703418G>T | CA406710490 | FUT2 | c.462G>T (p.Trp154Cys) n.431C>A | |
19 | g.48703419A>C | CA406710492 | FUT2 | c.463A>C (p.Thr155Pro) n.430T>G | |
19 | g.48703419A>G | CA406710494 | FUT2 | c.463A>G (p.Thr155Ala) n.430T>C | |
19 | g.48703419A>T | CA406710495 | FUT2 | c.463A>T (p.Thr155Ser) n.430T>A | |
19 | g.48703420C>A | CA406710497 | FUT2 | c.464C>A (p.Thr155Asn) n.429G>T | |
19 | g.48703420C= | CA2340030032 | FUT2 | c.464C= (p.Thr155=) n.429G= | |
19 | g.48703420C>G | CA406710499 | FUT2 | c.464C>G (p.Thr155Ser) n.429G>C | |
19 | g.48703420C>T | CA309352433 | FUT2 | c.464C>T (p.Thr155Ile) n.429G>A | dbSNP gnomAD v2 gnomAD v4 |
19 | g.48703420_48703423delinsCCTT | CA2340030033 | FUT2 | c.464_467delinsCCTT (p.Thr155=) n.426_429delinsAAGG | |
19 | g.48703420_48703421insTCT | CA2741636653 | FUT2 | c.464_465insTCT (p.Thr155_Phe156insLeu) n.428_429insAGA | |
19 | g.48703421C>A | CA508272563 | FUT2 | c.465C>A (p.Thr155=) n.428G>T | |
19 | g.48703421C>G | CA508272565 | FUT2 | c.465C>G (p.Thr155=) n.428G>C | |
19 | g.48703421C>T | CA508272567 | FUT2 | c.465C>T (p.Thr155=) n.428G>A | gnomAD v4 |
19 | g.48703423_48703425del | CA2340030034 | FUT2 | c.467_469del (p.Phe156del) n.426_428del | dbSNP |
19 | g.48703422T>A | CA406710504 | FUT2 | c.466T>A (p.Phe156Ile) n.427A>T | |
19 | g.48703422T>C | CA309352435 | FUT2 | c.466T>C (p.Phe156Leu) n.427A>G | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703422T>G | CA406710502 | FUT2 | c.466T>G (p.Phe156Val) n.427A>C | |
19 | g.48703422T= | CA2340030035 | FUT2 | c.466T= (p.Phe156=) n.427A= | |
19 | g.48703423T>A | CA406710507 | FUT2 | c.467T>A (p.Phe156Tyr) n.426A>T | |
19 | g.48703423T>C | CA406710509 | FUT2 | c.467T>C (p.Phe156Ser) n.426A>G | |
19 | g.48703423T>G | CA406710510 | FUT2 | c.467T>G (p.Phe156Cys) n.426A>C | |
19 | g.48703423_48703424insAC | CA2741636654 | FUT2 | c.467_468insAC (p.Phe156LeufsTer?) n.425_426insGT | |
19 | g.48703424C>A | CA406710513 | FUT2 | c.468C>A (p.Phe156Leu) n.425G>T | |
19 | g.48703424C>G | CA406710515 | FUT2 | c.468C>G (p.Phe156Leu) n.425G>C | |
19 | g.48703424C>T | CA508272574 | FUT2 | c.468C>T (p.Phe156=) n.425G>A | |
19 | g.48703425T>A | CA406710520 | FUT2 | c.469T>A (p.Tyr157Asn) n.424A>T | |
19 | g.48703425T>C | CA406710516 | FUT2 | c.469T>C (p.Tyr157His) n.424A>G | |
19 | g.48703425T>G | CA406710517 | FUT2 | c.469T>G (p.Tyr157Asp) n.424A>C | |
19 | g.48703425_48703426insCTTTAGTGAACACATTTTTAGGCAATTATAAGAAGCTGATTA | CA2741636655 | FUT2 | c.469_470insCTTTAGTGAACACATTTTTAGGCAATTATAAGAAGCTGATTA (p.Tyr157delinsSerLeuValAsnThrPheLeuGlyAsnTyrLysLysLeuIleAsn) n.423_424insTAATCAGCTTCTTATAATTGCCTAAAAATGTGTTCACTAAAG | |
19 | g.48703426A>C | CA406710523 | FUT2 | c.470A>C (p.Tyr157Ser) n.423T>G | |
19 | g.48703426A>G | CA406710525 | FUT2 | c.470A>G (p.Tyr157Cys) n.423T>C | |
19 | g.48703426A>T | CA406710527 | FUT2 | c.470A>T (p.Tyr157Phe) n.423T>A | |
19 | g.48703427C>A | CA406710529 | FUT2 | c.471C>A (p.Tyr157Ter) n.422G>T | |
19 | g.48703427C>G | CA406710534 | FUT2 | c.471C>G (p.Tyr157Ter) n.422G>C | |
19 | g.48703427C>T | CA508272576 | FUT2 | c.471C>T (p.Tyr157=) n.422G>A | |
19 | g.48703428del | CA2838856422 | FUT2 | c.472del (p.His158ThrfsTer30) n.422del | |
19 | g.48703428C>A | CA406710538 | FUT2 | c.472C>A (p.His158Asn) n.421G>T | |
19 | g.48703428C>G | CA406710549 | FUT2 | c.472C>G (p.His158Asp) n.421G>C | |
19 | g.48703428C>T | CA406710540 | FUT2 | c.472C>T (p.His158Tyr) n.421G>A | |
19 | g.48703429del | CA2843136254 | FUT2 | c.473del (p.His158ProfsTer30) n.420del | |
19 | g.48703429A= | CA2340030036 | FUT2 | c.473A= (p.His158=) n.420T= | |
19 | g.48703429A>C | CA406710553 | FUT2 | c.473A>C (p.His158Pro) n.420T>G | dbSNP |
19 | g.48703429A>G | CA406710554 | FUT2 | c.473A>G (p.His158Arg) n.420T>C | |
19 | g.48703429A>T | CA406710556 | FUT2 | c.473A>T (p.His158Leu) n.420T>A | |
19 | g.48703430C>A | CA406710558 | FUT2 | c.474C>A (p.His158Gln) n.419G>T | |
19 | g.48703430C= | CA2340030037 | FUT2 | c.474C= (p.His158=) n.419G= | |
19 | g.48703430C>G | CA406710560 | FUT2 | c.474C>G (p.His158Gln) n.419G>C | |
19 | g.48703430C>T | CA309352437 | FUT2 | c.474C>T (p.His158=) n.419G>A | dbSNP gnomAD v4 |
19 | g.48703431C>A | CA9556252 | FUT2 | c.475C>A (p.His159Asn) n.418G>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703431C= | CA2340030038 | FUT2 | c.475C= (p.His159=) n.418G= | |
19 | g.48703431C>G | CA406710566 | FUT2 | c.475C>G (p.His159Asp) n.418G>C | |
19 | g.48703431C>T | CA406710564 | FUT2 | c.475C>T (p.His159Tyr) n.418G>A | |
19 | g.48703432A= | CA2340030039 | FUT2 | c.476A= (p.His159=) n.417T= | |
19 | g.48703432A>C | CA406710572 | FUT2 | c.476A>C (p.His159Pro) n.417T>G | dbSNP gnomAD v4 |
19 | g.48703432A>G | CA406710574 | FUT2 | c.476A>G (p.His159Arg) n.417T>C | |
19 | g.48703432A>T | CA406710576 | FUT2 | c.476A>T (p.His159Leu) n.417T>A | |
19 | g.48703433C>A | CA406710579 | FUT2 | c.477C>A (p.His159Gln) n.416G>T | |
19 | g.48703433C= | CA2340030040 | FUT2 | c.477C= (p.His159=) n.416G= | |
19 | g.48703433C>G | CA406710581 | FUT2 | c.477C>G (p.His159Gln) n.416G>C | |
19 | g.48703433C>T | CA9556253 | FUT2 | c.477C>T (p.His159=) n.416G>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.48703434C>A | CA406710586 | FUT2 | c.478C>A (p.Leu160Ile) n.415G>T | COSMIC |
19 | g.48703434C>G | CA406710590 | FUT2 | c.478C>G (p.Leu160Val) n.415G>C | |
19 | g.48703434C>T | CA406710588 | FUT2 | c.478C>T (p.Leu160Phe) n.415G>A | |
19 | g.48703435T>A | CA406710592 | FUT2 | c.479T>A (p.Leu160His) n.414A>T | |
19 | g.48703435T>C | CA406710593 | FUT2 | c.479T>C (p.Leu160Pro) n.414A>G | |
19 | g.48703435T>G | CA406710594 | FUT2 | c.479T>G (p.Leu160Arg) n.414A>C | |
19 | g.48703436C>A | CA508272579 | FUT2 | c.480C>A (p.Leu160=) n.413G>T | gnomAD v4 |
19 | g.48703436C>G | CA508272580 | FUT2 | c.480C>G (p.Leu160=) n.413G>C | |
19 | g.48703436C>T | CA508272581 | FUT2 | c.480C>T (p.Leu160=) n.413G>A | |
19 | g.48703437C>A | CA406710597 | FUT2 | c.481C>A (p.Arg161Ser) n.412G>T | |
19 | g.48703437C= | CA2340030041 | FUT2 | c.481C= (p.Arg161=) n.412G= | |
19 | g.48703437C>G | CA406710600 | FUT2 | c.481C>G (p.Arg161Gly) n.412G>C | |
19 | g.48703437C>T | CA9556254 | FUT2 | c.481C>T (p.Arg161Cys) n.412G>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.48703438G>A | CA9556255 | FUT2 | c.482G>A (p.Arg161His) n.411C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703438G>C | CA406710604 | FUT2 | c.482G>C (p.Arg161Pro) n.411C>G | |
19 | g.48703438G= | CA2340030042 | FUT2 | c.482G= (p.Arg161=) n.411C= | |
19 | g.48703438G>T | CA406710607 | FUT2 | c.482G>T (p.Arg161Leu) n.411C>A | dbSNP gnomAD v2 |
19 | g.48703439C>A | CA508272582 | FUT2 | c.483C>A (p.Arg161=) n.410G>T | |
19 | g.48703439C>G | CA508272583 | FUT2 | c.483C>G (p.Arg161=) n.410G>C | |
19 | g.48703439C>T | CA508272584 | FUT2 | c.483C>T (p.Arg161=) n.410G>A | |
19 | g.48703439_48703440insAC | CA2555596717 | FUT2 | c.483_484insAC (p.Gln162ThrfsTer27) n.410_411insTG | |
19 | g.48703440dup | CA2843136255 | FUT2 | c.484dup (p.Gln162ProfsTer?) n.410dup | |
19 | g.48703440C>A | CA406710609 | FUT2 | c.484C>A (p.Gln162Lys) n.409G>T | |
19 | g.48703440C= | CA2340030043 | FUT2 | c.484C= (p.Gln162=) n.409G= | |
19 | g.48703440C>G | CA406710611 | FUT2 | c.484C>G (p.Gln162Glu) n.409G>C | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703440C>T | CA406710612 | FUT2 | c.484C>T (p.Gln162Ter) n.409G>A | |
19 | g.48703440_48703441del | CA2573032725 | FUT2 | c.484_485del (p.Gln162GlyfsTer?) n.408_409del | |
19 | g.48703441A>C | CA406710614 | FUT2 | c.485A>C (p.Gln162Pro) n.408T>G | |
19 | g.48703441A>G | CA406710617 | FUT2 | c.485A>G (p.Gln162Arg) n.408T>C | |
19 | g.48703441A>T | CA406710616 | FUT2 | c.485A>T (p.Gln162Leu) n.408T>A | |
19 | g.48703441_48703442del | CA2537245931 | FUT2 | c.485_486del (p.Gln162ArgfsTer?) n.407_408del | |
19 | g.48703442G>A | CA508272585 | FUT2 | c.486G>A (p.Gln162=) n.407C>T | gnomAD v4 |
19 | g.48703442G>C | CA9556256 | FUT2 | c.486G>C (p.Gln162His) n.407C>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.48703442G= | CA2340030044 | FUT2 | c.486G= (p.Gln162=) n.407C= | |
19 | g.48703442G>T | CA406710621 | FUT2 | c.486G>T (p.Gln162His) n.407C>A | |
19 | g.48703442_48703443insCC | CA2506093848 | FUT2 | c.486_487insCC (p.Glu163ProfsTer26) n.406_407insGG | |
19 | g.48703443G>A | CA406710623 | FUT2 | c.487G>A (p.Glu163Lys) n.406C>T | |
19 | g.48703443G>C | CA406710626 | FUT2 | c.487G>C (p.Glu163Gln) n.406C>G | |
19 | g.48703443G= | CA2340030045 | FUT2 | c.487G= (p.Glu163=) n.406C= | |
19 | g.48703443G>T | CA406710628 | FUT2 | c.487G>T (p.Glu163Ter) n.406C>A | dbSNP gnomAD v3 gnomAD v4 |
19 | g.48703444A>C | CA406710630 | FUT2 | c.488A>C (p.Glu163Ala) n.405T>G | |
19 | g.48703444A>G | CA406710632 | FUT2 | c.488A>G (p.Glu163Gly) n.405T>C | gnomAD v4 |
19 | g.48703444A>T | CA406710635 | FUT2 | c.488A>T (p.Glu163Val) n.405T>A | |
19 | g.48703445G>A | CA508272586 | FUT2 | c.489G>A (p.Glu163=) n.404C>T | |
19 | g.48703445G>C | CA406710638 | FUT2 | c.489G>C (p.Glu163Asp) n.404C>G | |
19 | g.48703445G>T | CA406710640 | FUT2 | c.489G>T (p.Glu163Asp) n.404C>A | |
19 | g.48703446A>C | CA406710643 | FUT2 | c.490A>C (p.Ile164Leu) n.403T>G | |
19 | g.48703446A>G | CA406710645 | FUT2 | c.490A>G (p.Ile164Val) n.403T>C | |
19 | g.48703446A>T | CA406710647 | FUT2 | c.490A>T (p.Ile164Phe) n.403T>A | |
19 | g.48703447T>A | CA406710648 | FUT2 | c.491T>A (p.Ile164Asn) n.402A>T | |
19 | g.48703447T>C | CA406710650 | FUT2 | c.491T>C (p.Ile164Thr) n.402A>G | |
19 | g.48703447T>G | CA406710649 | FUT2 | c.491T>G (p.Ile164Ser) n.402A>C | |
19 | g.48703448C>A | CA508272587 | FUT2 | c.492C>A (p.Ile164=) n.401G>T | |
19 | g.48703448C>G | CA406710652 | FUT2 | c.492C>G (p.Ile164Met) n.401G>C | |
19 | g.48703448C>T | CA508272588 | FUT2 | c.492C>T (p.Ile164=) n.401G>A | |
19 | g.48703449C>A | CA406710655 | FUT2 | c.493C>A (p.Leu165Ile) n.400G>T | |
19 | g.48703449C= | CA2340030046 | FUT2 | c.493C= (p.Leu165=) n.400G= | |
19 | g.48703449C>G | CA406710657 | FUT2 | c.493C>G (p.Leu165Val) n.400G>C | |
19 | g.48703449C>T | CA406710658 | FUT2 | c.493C>T (p.Leu165Phe) n.400G>A | dbSNP gnomAD v3 gnomAD v4 |
19 | g.48703450T>A | CA406710660 | FUT2 | c.494T>A (p.Leu165His) n.399A>T | |
19 | g.48703450T>C | CA406710663 | FUT2 | c.494T>C (p.Leu165Pro) n.399A>G | |
19 | g.48703450T>G | CA406710665 | FUT2 | c.494T>G (p.Leu165Arg) n.399A>C | |
19 | g.48703451C>A | CA508272589 | FUT2 | c.495C>A (p.Leu165=) n.398G>T | |
19 | g.48703451C>G | CA508272590 | FUT2 | c.495C>G (p.Leu165=) n.398G>C | |
19 | g.48703451C>T | CA508272591 | FUT2 | c.495C>T (p.Leu165=) n.398G>A | |
19 | g.48703452C>A | CA406710669 | FUT2 | c.496C>A (p.Gln166Lys) n.397G>T | |
19 | g.48703452C= | CA2340030047 | FUT2 | c.496C= (p.Gln166=) n.397G= | |
19 | g.48703452C>G | CA406710671 | FUT2 | c.496C>G (p.Gln166Glu) n.397G>C | |
19 | g.48703452C>T | CA9556257 | FUT2 | c.496C>T (p.Gln166Ter) n.397G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703453A= | CA2340030048 | FUT2 | c.497A= (p.Gln166=) n.396T= | |
19 | g.48703453A>C | CA406710674 | FUT2 | c.497A>C (p.Gln166Pro) n.396T>G | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703453A>G | CA406710677 | FUT2 | c.497A>G (p.Gln166Arg) n.396T>C | |
19 | g.48703453A>T | CA406710675 | FUT2 | c.497A>T (p.Gln166Leu) n.396T>A | |
19 | g.48703454G>A | CA508272592 | FUT2 | c.498G>A (p.Gln166=) n.395C>T | |
19 | g.48703454G>C | CA406710683 | FUT2 | c.498G>C (p.Gln166His) n.395C>G | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703454G= | CA2340030049 | FUT2 | c.498G= (p.Gln166=) n.395C= | |
19 | g.48703454G>T | CA406710685 | FUT2 | c.498G>T (p.Gln166His) n.395C>A | |
19 | g.48703455G>A | CA9556258 | FUT2 | c.499G>A (p.Glu167Lys) n.394C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.48703455G>C | CA406710688 | FUT2 | c.499G>C (p.Glu167Gln) n.394C>G | |
19 | g.48703455G= | CA2340030050 | FUT2 | c.499G= (p.Glu167=) n.394C= | |
19 | g.48703455G>T | CA406710687 | FUT2 | c.499G>T (p.Glu167Ter) n.394C>A | |
19 | g.48703456A>C | CA406710692 | FUT2 | c.500A>C (p.Glu167Ala) n.393T>G | |
19 | g.48703456A>G | CA406710694 | FUT2 | c.500A>G (p.Glu167Gly) n.393T>C | |
19 | g.48703456A>T | CA406710696 | FUT2 | c.500A>T (p.Glu167Val) n.393T>A | |
19 | g.48703457G>A | CA508272593 | FUT2 | c.501G>A (p.Glu167=) n.392C>T | |
19 | g.48703457G>C | CA406710698 | FUT2 | c.501G>C (p.Glu167Asp) n.392C>G | |
19 | g.48703457G>T | CA406710700 | FUT2 | c.501G>T (p.Glu167Asp) n.392C>A | |
19 | g.48703458T>A | CA406710703 | FUT2 | c.502T>A (p.Phe168Ile) n.391A>T | |
19 | g.48703458T>C | CA406710705 | FUT2 | c.502T>C (p.Phe168Leu) n.391A>G | |
19 | g.48703458T>G | CA406710707 | FUT2 | c.502T>G (p.Phe168Val) n.391A>C | gnomAD v4 |
19 | g.48703459T>A | CA406710710 | FUT2 | c.503T>A (p.Phe168Tyr) n.390A>T | |
19 | g.48703459T>C | CA406710711 | FUT2 | c.503T>C (p.Phe168Ser) n.390A>G | |
19 | g.48703459T>G | CA406710713 | FUT2 | c.503T>G (p.Phe168Cys) n.390A>C | |
19 | g.48703460C>A | CA406710717 | FUT2 | c.504C>A (p.Phe168Leu) n.389G>T | |
19 | g.48703460C= | CA2340030051 | FUT2 | c.504C= (p.Phe168=) n.389G= | |
19 | g.48703460C>G | CA406710716 | FUT2 | c.504C>G (p.Phe168Leu) n.389G>C | |
19 | g.48703460C>T | CA508272594 | FUT2 | c.504C>T (p.Phe168=) n.389G>A | dbSNP gnomAD v4 |
19 | g.48703461A= | CA2340030052 | FUT2 | c.505A= (p.Thr169=) n.388T= | |
19 | g.48703461A>C | CA406710721 | FUT2 | c.505A>C (p.Thr169Pro) n.388T>G | dbSNP |
19 | g.48703461A>G | CA406710723 | FUT2 | c.505A>G (p.Thr169Ala) n.388T>C | |
19 | g.48703461A>T | CA406710725 | FUT2 | c.505A>T (p.Thr169Ser) n.388T>A | |
19 | g.48703462C>A | CA406710727 | FUT2 | c.506C>A (p.Thr169Asn) n.387G>T | |
19 | g.48703462C= | CA2340030053 | FUT2 | c.506C= (p.Thr169=) n.387G= | |
19 | g.48703462C>G | CA406710729 | FUT2 | c.506C>G (p.Thr169Ser) n.387G>C | |
19 | g.48703462C>T | CA406710731 | FUT2 | c.506C>T (p.Thr169Ile) n.387G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |