Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
16 | g.67940395G>A | CA396376260 | LCAT | c.832C>T (p.Pro278Ser) c.156-321C>T c.616C>T (p.Pro206Ser) c.570C>T (n.570C>T) | ClinVar dbSNP gnomAD v4 COSMIC |
16 | g.67940395G>C | CA396376261 | LCAT | c.832C>G (p.Pro278Ala) c.156-321C>G c.616C>G (p.Pro206Ala) c.570C>G (n.570C>G) | |
16 | g.67940395G= | CA2229563340 | LCAT | c.832C= (p.Pro278=) c.156-321C= c.616C= (p.Pro206=) c.570C= (n.570C=) | |
16 | g.67940395G>T | CA396376262 | LCAT | c.832C>A (p.Pro278Thr) c.156-321C>A c.616C>A (p.Pro206Thr) c.570C>A (n.570C>A) | |
16 | g.67940396A>C | CA396376263 | LCAT | c.831T>G (p.Phe277Leu) c.156-322T>G c.615T>G (p.Phe205Leu) c.569T>G (n.569T>G) | |
16 | g.67940396A>G | CA496384027 | LCAT | c.831T>C (p.Phe277=) c.156-322T>C c.615T>C (p.Phe205=) c.569T>C (n.569T>C) | gnomAD v4 |
16 | g.67940396A>T | CA396376264 | LCAT | c.831T>A (p.Phe277Leu) c.156-322T>A c.615T>A (p.Phe205Leu) c.569T>A (n.569T>A) | |
16 | g.67940397A>C | CA396376267 | LCAT | c.830T>G (p.Phe277Cys) c.156-323T>G c.614T>G (p.Phe205Cys) c.568T>G (n.568T>G) | |
16 | g.67940397A>G | CA396376266 | LCAT | c.830T>C (p.Phe277Ser) c.156-323T>C c.614T>C (p.Phe205Ser) c.568T>C (n.568T>C) | |
16 | g.67940397A>T | CA396376265 | LCAT | c.830T>A (p.Phe277Tyr) c.156-323T>A c.614T>A (p.Phe205Tyr) c.568T>A (n.568T>A) | |
16 | g.67940398A>C | CA396376268 | LCAT | c.829T>G (p.Phe277Val) c.156-324T>G c.613T>G (p.Phe205Val) c.567T>G (n.567T>G) | |
16 | g.67940398A>G | CA396376269 | LCAT | c.829T>C (p.Phe277Leu) c.156-324T>C c.613T>C (p.Phe205Leu) c.567T>C (n.567T>C) | |
16 | g.67940398A>T | CA396376270 | LCAT | c.829T>A (p.Phe277Ile) c.156-324T>A c.613T>A (p.Phe205Ile) c.567T>A (n.567T>A) | |
16 | g.67940399_67940400dup | CA2554837458 | LCAT | c.828_829dup (p.Phe277CysfsTer?) c.156-325_156-324dup c.612_613dup (p.Phe205CysfsTer?) c.566_567dup (n.566_567dup) | |
16 | g.67940399C>A | CA396376271 | LCAT | c.828G>T (p.Met276Ile) c.156-325G>T c.612G>T (p.Met204Ile) c.566G>T (n.566G>T) | |
16 | g.67940399C= | CA2229563341 | LCAT | c.828G= (p.Met276=) c.156-325G= c.612G= (p.Met204=) c.566G= (n.566G=) | |
16 | g.67940399C>G | CA396376272 | LCAT | c.828G>C (p.Met276Ile) c.156-325G>C c.612G>C (p.Met204Ile) c.566G>C (n.566G>C) | |
16 | g.67940399C>T | CA8120950 | LCAT | c.828G>A (p.Met276Ile) c.156-325G>A c.612G>A (p.Met204Ile) c.566G>A (n.566G>A) | dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.67940400A= | CA2229563342 | LCAT | c.827T= (p.Met276=) c.156-326T= c.611T= (p.Met204=) c.565T= (n.565T=) | |
16 | g.67940400A>C | CA396376274 | LCAT | c.827T>G (p.Met276Arg) c.156-326T>G c.611T>G (p.Met204Arg) c.565T>G (n.565T>G) | |
16 | g.67940400A>G | CA396376273 | LCAT | c.827T>C (p.Met276Thr) c.156-326T>C c.611T>C (p.Met204Thr) c.565T>C (n.565T>C) | dbSNP gnomAD v2 gnomAD v4 |
16 | g.67940400A>T | CA116421 | LCAT | c.827T>A (p.Met276Lys) c.156-326T>A c.611T>A (p.Met204Lys) c.565T>A (n.565T>A) | ClinVar dbSNP gnomAD v4 |
16 | g.67940401T>A | CA396376275 | LCAT | c.826A>T (p.Met276Leu) c.156-327A>T c.610A>T (p.Met204Leu) c.564A>T (n.564A>T) | |
16 | g.67940401T>C | CA396376276 | LCAT | c.826A>G (p.Met276Val) c.156-327A>G c.610A>G (p.Met204Val) c.564A>G (n.564A>G) | |
16 | g.67940401T>G | CA396376277 | LCAT | c.826A>C (p.Met276Leu) c.156-327A>C c.610A>C (p.Met204Leu) c.564A>C (n.564A>C) | |
16 | g.67940402C>A | CA396376278 | LCAT | c.825G>T (p.Trp275Cys) c.156-328G>T c.609G>T (p.Trp203Cys) c.563G>T (n.563G>T) | |
16 | g.67940402C>G | CA396376279 | LCAT | c.825G>C (p.Trp275Cys) c.156-328G>C c.609G>C (p.Trp203Cys) c.563G>C (n.563G>C) | |
16 | g.67940402C>T | CA396376280 | LCAT | c.825G>A (p.Trp275Ter) c.156-328G>A c.609G>A (p.Trp203Ter) c.563G>A (n.563G>A) | |
16 | g.67940403C>A | CA396376281 | LCAT | c.824G>T (p.Trp275Leu) c.156-329G>T c.608G>T (p.Trp203Leu) c.562G>T (n.562G>T) | |
16 | g.67940403C>G | CA396376282 | LCAT | c.824G>C (p.Trp275Ser) c.156-329G>C c.608G>C (p.Trp203Ser) c.562G>C (n.562G>C) | COSMIC |
16 | g.67940403C>T | CA396376283 | LCAT | c.824G>A (p.Trp275Ter) c.156-329G>A c.608G>A (p.Trp203Ter) c.562G>A (n.562G>A) | gnomAD v4 |
16 | g.67940404A>C | CA396376284 | LCAT | c.823T>G (p.Trp275Gly) c.156-330T>G c.607T>G (p.Trp203Gly) c.561T>G (n.561T>G) | |
16 | g.67940404A>G | CA396376285 | LCAT | c.823T>C (p.Trp275Arg) c.156-330T>C c.607T>C (p.Trp203Arg) c.561T>C (n.561T>C) | |
16 | g.67940404A>T | CA396376286 | LCAT | c.823T>A (p.Trp275Arg) c.156-330T>A c.607T>A (p.Trp203Arg) c.561T>A (n.561T>A) | |
16 | g.67940405G>A | CA496384028 | LCAT | c.822C>T (p.Pro274=) c.156-331C>T c.606C>T (p.Pro202=) c.560C>T (n.560C>T) | |
16 | g.67940405G>C | CA496384029 | LCAT | c.822C>G (p.Pro274=) c.156-331C>G c.606C>G (p.Pro202=) c.560C>G (n.560C>G) | |
16 | g.67940405G>T | CA496384030 | LCAT | c.822C>A (p.Pro274=) c.156-331C>A c.606C>A (p.Pro202=) c.560C>A (n.560C>A) | |
16 | g.67940406G>A | CA396376289 | LCAT | c.821C>T (p.Pro274Leu) c.156-332C>T c.605C>T (p.Pro202Leu) c.559C>T (n.559C>T) | |
16 | g.67940406G>C | CA396376287 | LCAT | c.821C>G (p.Pro274Arg) c.156-332C>G c.605C>G (p.Pro202Arg) c.559C>G (n.559C>G) | dbSNP gnomAD v4 |
16 | g.67940406G= | CA2229563343 | LCAT | c.821C= (p.Pro274=) c.156-332C= c.605C= (p.Pro202=) c.559C= (n.559C=) | |
16 | g.67940406G>T | CA396376288 | LCAT | c.821C>A (p.Pro274His) c.156-332C>A c.605C>A (p.Pro202His) c.559C>A (n.559C>A) | |
16 | g.67940407G>A | CA396376290 | LCAT | c.820C>T (p.Pro274Ser) c.156-333C>T c.604C>T (p.Pro202Ser) c.558C>T (n.558C>T) | |
16 | g.67940407G>C | CA396376291 | LCAT | c.820C>G (p.Pro274Ala) c.156-333C>G c.604C>G (p.Pro202Ala) c.558C>G (n.558C>G) | |
16 | g.67940407G>T | CA396376292 | LCAT | c.820C>A (p.Pro274Thr) c.156-333C>A c.604C>A (p.Pro202Thr) c.558C>A (n.558C>A) | |
16 | g.67940408G>A | CA496384031 | LCAT | c.819C>T (p.Ser273=) c.156-334C>T c.603C>T (p.Ser201=) c.557C>T (n.557C>T) | ClinVar gnomAD v4 |
16 | g.67940408G>C | CA496384032 | LCAT | c.819C>G (p.Ser273=) c.156-334C>G c.603C>G (p.Ser201=) c.557C>G (n.557C>G) | |
16 | g.67940408G>T | CA496384033 | LCAT | c.819C>A (p.Ser273=) c.156-334C>A c.603C>A (p.Ser201=) c.557C>A (n.557C>A) | gnomAD v4 |
16 | g.67940409G>A | CA396376293 | LCAT | c.818C>T (p.Ser273Phe) c.156-335C>T c.602C>T (p.Ser201Phe) c.556C>T (n.556C>T) | |
16 | g.67940409G>C | CA396376294 | LCAT | c.818C>G (p.Ser273Cys) c.156-335C>G c.602C>G (p.Ser201Cys) c.556C>G (n.556C>G) | |
16 | g.67940409G>T | CA396376295 | LCAT | c.818C>A (p.Ser273Tyr) c.156-335C>A c.602C>A (p.Ser201Tyr) c.556C>A (n.556C>A) | |
16 | g.67940410A>C | CA396376296 | LCAT | c.817T>G (p.Ser273Ala) c.156-336T>G c.601T>G (p.Ser201Ala) c.555T>G (n.555T>G) | |
16 | g.67940410A>G | CA396376297 | LCAT | c.817T>C (p.Ser273Pro) c.156-336T>C c.601T>C (p.Ser201Pro) c.555T>C (n.555T>C) | |
16 | g.67940410A>T | CA396376298 | LCAT | c.817T>A (p.Ser273Thr) c.156-336T>A c.601T>A (p.Ser201Thr) c.555T>A (n.555T>A) | |
16 | g.67940411G>A | CA496384034 | LCAT | c.816C>T (p.Thr272=) c.156-337C>T c.600C>T (p.Thr200=) c.554C>T (n.554C>T) | dbSNP gnomAD v2 gnomAD v4 |
16 | g.67940411G>C | CA496384036 | LCAT | c.816C>G (p.Thr272=) c.156-337C>G c.600C>G (p.Thr200=) c.554C>G (n.554C>G) | |
16 | g.67940411G= | CA2229563344 | LCAT | c.816C= (p.Thr272=) c.156-337C= c.600C= (p.Thr200=) c.554C= (n.554C=) | |
16 | g.67940411G>T | CA496384035 | LCAT | c.816C>A (p.Thr272=) c.156-337C>A c.600C>A (p.Thr200=) c.554C>A (n.554C>A) | COSMIC |
16 | g.67940417_67940419del | CA2633851016 | LCAT | c.814_816del (p.Thr272del) c.156-339_156-337del c.598_600del (p.Thr200del) c.552_554del (n.552_554del) | gnomAD v4 |
16 | g.67940412G>A | CA396376299 | LCAT | c.815C>T (p.Thr272Ile) c.156-338C>T c.599C>T (p.Thr200Ile) c.553C>T (n.553C>T) | dbSNP |
16 | g.67940412G>C | CA396376300 | LCAT | c.815C>G (p.Thr272Ser) c.156-338C>G c.599C>G (p.Thr200Ser) c.553C>G (n.553C>G) | |
16 | g.67940412G= | CA2229563345 | LCAT | c.815C= (p.Thr272=) c.156-338C= c.599C= (p.Thr200=) c.553C= (n.553C=) | |
16 | g.67940412G>T | CA396376301 | LCAT | c.815C>A (p.Thr272Asn) c.156-338C>A c.599C>A (p.Thr200Asn) c.553C>A (n.553C>A) | |
16 | g.67940413T>A | CA396376304 | LCAT | c.814A>T (p.Thr272Ser) c.156-339A>T c.598A>T (p.Thr200Ser) c.552A>T (n.552A>T) | |
16 | g.67940413T>C | CA396376303 | LCAT | c.814A>G (p.Thr272Ala) c.156-339A>G c.598A>G (p.Thr200Ala) c.552A>G (n.552A>G) | gnomAD v4 |
16 | g.67940413T>G | CA396376302 | LCAT | c.814A>C (p.Thr272Pro) c.156-339A>C c.598A>C (p.Thr200Pro) c.552A>C (n.552A>C) | |
16 | g.67940414G>A | CA496384037 | LCAT | c.813C>T (p.Thr271=) c.156-340C>T c.597C>T (p.Thr199=) c.551C>T (n.551C>T) | |
16 | g.67940414G>C | CA496384038 | LCAT | c.813C>G (p.Thr271=) c.156-340C>G c.597C>G (p.Thr199=) c.551C>G (n.551C>G) | |
16 | g.67940414G>T | CA496384039 | LCAT | c.813C>A (p.Thr271=) c.156-340C>A c.597C>A (p.Thr199=) c.551C>A (n.551C>A) | |
16 | g.67940415G>A | CA396376305 | LCAT | c.812C>T (p.Thr271Ile) c.156-341C>T c.596C>T (p.Thr199Ile) c.550C>T (n.550C>T) | |
16 | g.67940415G>C | CA396376306 | LCAT | c.812C>G (p.Thr271Ser) c.156-341C>G c.596C>G (p.Thr199Ser) c.550C>G (n.550C>G) | |
16 | g.67940415G>T | CA396376307 | LCAT | c.812C>A (p.Thr271Asn) c.156-341C>A c.596C>A (p.Thr199Asn) c.550C>A (n.550C>A) | |
16 | g.67940416T>A | CA396376308 | LCAT | c.811A>T (p.Thr271Ser) c.156-342A>T c.595A>T (p.Thr199Ser) c.549A>T (n.549A>T) | |
16 | g.67940416T>C | CA396376309 | LCAT | c.811A>G (p.Thr271Ala) c.156-342A>G c.595A>G (p.Thr199Ala) c.549A>G (n.549A>G) | |
16 | g.67940416T>G | CA396376310 | LCAT | c.811A>C (p.Thr271Pro) c.156-342A>C c.595A>C (p.Thr199Pro) c.549A>C (n.549A>C) | |
16 | g.67940417G>A | CA496384040 | LCAT | c.810C>T (p.Thr270=) c.156-343C>T c.594C>T (p.Thr198=) c.548C>T (n.548C>T) | dbSNP gnomAD v4 |
16 | g.67940417G>C | CA496384041 | LCAT | c.810C>G (p.Thr270=) c.156-343C>G c.594C>G (p.Thr198=) c.548C>G (n.548C>G) | |
16 | g.67940417G>T | CA496384042 | LCAT | c.810C>A (p.Thr270=) c.156-343C>A c.594C>A (p.Thr198=) c.548C>A (n.548C>A) | |
16 | g.67940418G>A | CA8120951 | LCAT | c.809C>T (p.Thr270Ile) c.156-344C>T c.593C>T (p.Thr198Ile) c.547C>T (n.547C>T) | dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.67940418G>C | CA396376311 | LCAT | c.809C>G (p.Thr270Ser) c.156-344C>G c.593C>G (p.Thr198Ser) c.547C>G (n.547C>G) | |
16 | g.67940418G= | CA2229563346 | LCAT | c.809C= (p.Thr270=) c.156-344C= c.593C= (p.Thr198=) c.547C= (n.547C=) | |
16 | g.67940418G>T | CA396376312 | LCAT | c.809C>A (p.Thr270Asn) c.156-344C>A c.593C>A (p.Thr198Asn) c.547C>A (n.547C>A) | |
16 | g.67940419T>A | CA396376313 | LCAT | c.808A>T (p.Thr270Ser) c.156-345A>T c.592A>T (p.Thr198Ser) c.546A>T (n.546A>T) | |
16 | g.67940419T>C | CA396376314 | LCAT | c.808A>G (p.Thr270Ala) c.156-345A>G c.592A>G (p.Thr198Ala) c.546A>G (n.546A>G) | |
16 | g.67940419T>G | CA396376315 | LCAT | c.808A>C (p.Thr270Pro) c.156-345A>C c.592A>C (p.Thr198Pro) c.546A>C (n.546A>C) | |
16 | g.67940420T>A | CA496384043 | LCAT | c.807A>T (p.Ile269=) c.156-346A>T c.591A>T (p.Ile197=) c.545A>T (n.545A>T) | |
16 | g.67940420T>C | CA396376316 | LCAT | c.807A>G (p.Ile269Met) c.156-346A>G c.591A>G (p.Ile197Met) c.545A>G (n.545A>G) | |
16 | g.67940420T>G | CA496384044 | LCAT | c.807A>C (p.Ile269=) c.156-346A>C c.591A>C (p.Ile197=) c.545A>C (n.545A>C) | |
16 | g.67940421A>C | CA396376318 | LCAT | c.806T>G (p.Ile269Arg) c.156-347T>G c.590T>G (p.Ile197Arg) c.544T>G (n.544T>G) | |
16 | g.67940421A>G | CA396376319 | LCAT | c.806T>C (p.Ile269Thr) c.156-347T>C c.590T>C (p.Ile197Thr) c.544T>C (n.544T>C) | |
16 | g.67940421A>T | CA396376317 | LCAT | c.806T>A (p.Ile269Lys) c.156-347T>A c.590T>A (p.Ile197Lys) c.544T>A (n.544T>A) | |
16 | g.67940422T>A | CA396376320 | LCAT | c.805A>T (p.Ile269Leu) c.156-348A>T c.589A>T (p.Ile197Leu) c.543A>T (n.543A>T) | |
16 | g.67940422T>C | CA283161018 | LCAT | c.805A>G (p.Ile269Val) c.156-348A>G c.589A>G (p.Ile197Val) c.543A>G (n.543A>G) | dbSNP |
16 | g.67940422T>G | CA396376321 | LCAT | c.805A>C (p.Ile269Leu) c.156-348A>C c.589A>C (p.Ile197Leu) c.543A>C (n.543A>C) | |
16 | g.67940422T= | CA2229563347 | LCAT | c.805A= (p.Ile269=) c.156-348A= c.589A= (p.Ile197=) c.543A= (n.543A=) | |
16 | g.67940423G>A | CA496384045 | LCAT | c.804C>T (p.Arg268=) c.156-349C>T c.588C>T (p.Arg196=) c.542C>T (n.542C>T) | gnomAD v4 |
16 | g.67940423G>C | CA496384046 | LCAT | c.804C>G (p.Arg268=) c.156-349C>G c.588C>G (p.Arg196=) c.542C>G (n.542C>G) | |
16 | g.67940423G>T | CA496384047 | LCAT | c.804C>A (p.Arg268=) c.156-349C>A c.588C>A (p.Arg196=) c.542C>A (n.542C>A) | |
16 | g.67940424C>A | CA396376322 | LCAT | c.803G>T (p.Arg268Leu) c.156-350G>T c.587G>T (p.Arg196Leu) c.541G>T (n.541G>T) | |
16 | g.67940424C= | CA2229563348 | LCAT | c.803G= (p.Arg268=) c.156-350G= c.587G= (p.Arg196=) c.541G= (n.541G=) | |
16 | g.67940424C>G | CA396376323 | LCAT | c.803G>C (p.Arg268Pro) c.156-350G>C c.587G>C (p.Arg196Pro) c.541G>C (n.541G>C) | gnomAD v4 |
16 | g.67940424C>T | CA8120952 | LCAT | c.803G>A (p.Arg268His) c.156-350G>A c.587G>A (p.Arg196His) c.541G>A (n.541G>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.67940425G>A | CA8120954 | LCAT | c.802C>T (p.Arg268Cys) c.156-351C>T c.586C>T (p.Arg196Cys) c.540C>T (n.540C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.67940425G>C | CA396376324 | LCAT | c.802C>G (p.Arg268Gly) c.156-351C>G c.586C>G (p.Arg196Gly) c.540C>G (n.540C>G) | |
16 | g.67940425G= | CA2229563349 | LCAT | c.802C= (p.Arg268=) c.156-351C= c.586C= (p.Arg196=) c.540C= (n.540C=) | |
16 | g.67940425G>T | CA8120953 | LCAT | c.802C>A (p.Arg268Ser) c.156-351C>A c.586C>A (p.Arg196Ser) c.540C>A (n.540C>A) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.67940426C>A | CA396376325 | LCAT | c.801G>T (p.Gln267His) c.156-352G>T c.585G>T (p.Gln195His) c.539G>T (n.539G>T) | |
16 | g.67940426C= | CA2229563350 | LCAT | c.801G= (p.Gln267=) c.156-352G= c.585G= (p.Gln195=) c.539G= (n.539G=) | |
16 | g.67940426C>G | CA396376326 | LCAT | c.801G>C (p.Gln267His) c.156-352G>C c.585G>C (p.Gln195His) c.539G>C (n.539G>C) | |
16 | g.67940426C>T | CA496384048 | LCAT | c.801G>A (p.Gln267=) c.156-352G>A c.585G>A (p.Gln195=) c.539G>A (n.539G>A) | dbSNP gnomAD v4 |
16 | g.67940428_67940435del | CA2695223583 | LCAT | c.794_801del (p.Glu265AlafsTer18) c.156-359_156-352del c.578_585del (p.Glu193AlafsTer18) c.532_539del (n.532_539del) | |
16 | g.67940427T>A | CA396376327 | LCAT | c.800A>T (p.Gln267Leu) c.156-353A>T c.584A>T (p.Gln195Leu) c.538A>T (n.538A>T) | |
16 | g.67940427T>C | CA396376328 | LCAT | c.800A>G (p.Gln267Arg) c.156-353A>G c.584A>G (p.Gln195Arg) c.538A>G (n.538A>G) | |
16 | g.67940427T>G | CA396376329 | LCAT | c.800A>C (p.Gln267Pro) c.156-353A>C c.584A>C (p.Gln195Pro) c.538A>C (n.538A>C) | |
16 | g.67940428G>A | CA8120955 | LCAT | c.799C>T (p.Gln267Ter) c.156-354C>T c.583C>T (p.Gln195Ter) c.537C>T (n.537C>T) | dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.67940428G>C | CA396376330 | LCAT | c.799C>G (p.Gln267Glu) c.156-354C>G c.583C>G (p.Gln195Glu) c.537C>G (n.537C>G) | |
16 | g.67940428G= | CA2229563351 | LCAT | c.799C= (p.Gln267=) c.156-354C= c.583C= (p.Gln195=) c.537C= (n.537C=) | |
16 | g.67940428G>T | CA396376331 | LCAT | c.799C>A (p.Gln267Lys) c.156-354C>A c.583C>A (p.Gln195Lys) c.537C>A (n.537C>A) | |
16 | g.67940429C>A | CA396376333 | LCAT | c.798G>T (p.Glu266Asp) c.156-355G>T c.582G>T (p.Glu194Asp) c.536G>T (n.536G>T) | |
16 | g.67940429C>G | CA396376332 | LCAT | c.798G>C (p.Glu266Asp) c.156-355G>C c.582G>C (p.Glu194Asp) c.536G>C (n.536G>C) | |
16 | g.67940429C>T | CA496384049 | LCAT | c.798G>A (p.Glu266=) c.156-355G>A c.582G>A (p.Glu194=) c.536G>A (n.536G>A) | |
16 | g.67940430T>A | CA396376334 | LCAT | c.797A>T (p.Glu266Val) c.156-356A>T c.581A>T (p.Glu194Val) c.535A>T (n.535A>T) | |
16 | g.67940430T>C | CA396376335 | LCAT | c.797A>G (p.Glu266Gly) c.156-356A>G c.581A>G (p.Glu194Gly) c.535A>G (n.535A>G) | |
16 | g.67940430T>G | CA396376336 | LCAT | c.797A>C (p.Glu266Ala) c.156-356A>C c.581A>C (p.Glu194Ala) c.535A>C (n.535A>C) | |
16 | g.67940431C>A | CA396376337 | LCAT | c.796G>T (p.Glu266Ter) c.156-357G>T c.580G>T (p.Glu194Ter) c.534G>T (n.534G>T) | |
16 | g.67940431C>G | CA396376338 | LCAT | c.796G>C (p.Glu266Gln) c.156-357G>C c.580G>C (p.Glu194Gln) c.534G>C (n.534G>C) | |
16 | g.67940431C>T | CA396376339 | LCAT | c.796G>A (p.Glu266Lys) c.156-357G>A c.580G>A (p.Glu194Lys) c.534G>A (n.534G>A) | ClinVar |
16 | g.67940432C>A | CA396376340 | LCAT | c.795G>T (p.Glu265Asp) c.156-358G>T c.579G>T (p.Glu193Asp) c.533G>T (n.533G>T) | dbSNP gnomAD v2 |
16 | g.67940432C= | CA2229563352 | LCAT | c.795G= (p.Glu265=) c.156-358G= c.579G= (p.Glu193=) c.533G= (n.533G=) | |
16 | g.67940432C>G | CA396376341 | LCAT | c.795G>C (p.Glu265Asp) c.156-358G>C c.579G>C (p.Glu193Asp) c.533G>C (n.533G>C) | gnomAD v4 |
16 | g.67940432C>T | CA496384050 | LCAT | c.795G>A (p.Glu265=) c.156-358G>A c.579G>A (p.Glu193=) c.533G>A (n.533G>A) | ClinVar |
16 | g.67940433T>A | CA396376342 | LCAT | c.794A>T (p.Glu265Val) c.156-359A>T c.578A>T (p.Glu193Val) c.532A>T (n.532A>T) | |
16 | g.67940433T>C | CA396376343 | LCAT | c.794A>G (p.Glu265Gly) c.156-359A>G c.578A>G (p.Glu193Gly) c.532A>G (n.532A>G) | gnomAD v4 |
16 | g.67940433T>G | CA396376344 | LCAT | c.794A>C (p.Glu265Ala) c.156-359A>C c.578A>C (p.Glu193Ala) c.532A>C (n.532A>C) | |
16 | g.67940434C>A | CA396376346 | LCAT | c.793G>T (p.Glu265Ter) c.156-360G>T c.577G>T (p.Glu193Ter) c.531G>T (n.531G>T) | |
16 | g.67940434C>G | CA396376347 | LCAT | c.793G>C (p.Glu265Gln) c.156-360G>C c.577G>C (p.Glu193Gln) c.531G>C (n.531G>C) | |
16 | g.67940434C>T | CA396376345 | LCAT | c.793G>A (p.Glu265Lys) c.156-360G>A c.577G>A (p.Glu193Lys) c.531G>A (n.531G>A) | |
16 | g.67940435T>A | CA396376348 | LCAT | c.792A>T (p.Lys264Asn) c.156-361A>T c.576A>T (p.Lys192Asn) c.530A>T (n.530A>T) | |
16 | g.67940435T>C | CA496384051 | LCAT | c.792A>G (p.Lys264=) c.156-361A>G c.576A>G (p.Lys192=) c.530A>G (n.530A>G) | |
16 | g.67940435T>G | CA396376349 | LCAT | c.792A>C (p.Lys264Asn) c.156-361A>C c.576A>C (p.Lys192Asn) c.530A>C (n.530A>C) | |
16 | g.67940436T>A | CA396376350 | LCAT | c.791A>T (p.Lys264Ile) c.156-362A>T c.575A>T (p.Lys192Ile) c.529A>T (n.529A>T) | |
16 | g.67940436T>C | CA396376351 | LCAT | c.791A>G (p.Lys264Arg) c.156-362A>G c.575A>G (p.Lys192Arg) c.529A>G (n.529A>G) | |
16 | g.67940436T>G | CA396376352 | LCAT | c.791A>C (p.Lys264Thr) c.156-362A>C c.575A>C (p.Lys192Thr) c.529A>C (n.529A>C) | |
16 | g.67940437T>A | CA396376353 | LCAT | c.790A>T (p.Lys264Ter) c.156-363A>T c.574A>T (p.Lys192Ter) c.528A>T (n.528A>T) | |
16 | g.67940437T>C | CA283161039 | LCAT | c.790A>G (p.Lys264Glu) c.156-363A>G c.574A>G (p.Lys192Glu) c.528A>G (n.528A>G) | dbSNP |
16 | g.67940437T>G | CA396376354 | LCAT | c.790A>C (p.Lys264Gln) c.156-363A>C c.574A>C (p.Lys192Gln) c.528A>C (n.528A>C) | |
16 | g.67940437T= | CA2229563353 | LCAT | c.790A= (p.Lys264=) c.156-363A= c.574A= (p.Lys192=) c.528A= (n.528A=) | |
16 | g.67940438C>A | CA496384052 | LCAT | c.789G>T (p.Leu263=) c.156-364G>T c.573G>T (p.Leu191=) c.527G>T (n.527G>T) | |
16 | g.67940438C= | CA2229563354 | LCAT | c.789G= (p.Leu263=) c.156-364G= c.573G= (p.Leu191=) c.527G= (n.527G=) | |
16 | g.67940438C>G | CA496384053 | LCAT | c.789G>C (p.Leu263=) c.156-364G>C c.573G>C (p.Leu191=) c.527G>C (n.527G>C) | |
16 | g.67940438C>T | CA496384054 | LCAT | c.789G>A (p.Leu263=) c.156-364G>A c.573G>A (p.Leu191=) c.527G>A (n.527G>A) | dbSNP |
16 | g.67940439A= | CA2229563355 | LCAT | c.788T= (p.Leu263=) c.156-365T= c.572T= (p.Leu191=) c.526T= (n.526T=) | |
16 | g.67940439A>C | CA396376355 | LCAT | c.788T>G (p.Leu263Arg) c.156-365T>G c.572T>G (p.Leu191Arg) c.526T>G (n.526T>G) | |
16 | g.67940439A>G | CA396376356 | LCAT | c.788T>C (p.Leu263Pro) c.156-365T>C c.572T>C (p.Leu191Pro) c.526T>C (n.526T>C) | |
16 | g.67940439A>T | CA8120956 | LCAT | c.788T>A (p.Leu263Gln) c.156-365T>A c.572T>A (p.Leu191Gln) c.526T>A (n.526T>A) | dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.67940440G>A | CA8120957 | LCAT | c.787C>T (p.Leu263=) c.156-366C>T c.571C>T (p.Leu191=) c.525C>T (n.525C>T) | dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.67940440G>C | CA396376358 | LCAT | c.787C>G (p.Leu263Val) c.156-366C>G c.571C>G (p.Leu191Val) c.525C>G (n.525C>G) | |
16 | g.67940440G= | CA2229563356 | LCAT | c.787C= (p.Leu263=) c.156-366C= c.571C= (p.Leu191=) c.525C= (n.525C=) | |
16 | g.67940440G>T | CA396376357 | LCAT | c.787C>A (p.Leu263Met) c.156-366C>A c.571C>A (p.Leu191Met) c.525C>A (n.525C>A) | |
16 | g.67940441C>A | CA396376359 | LCAT | c.786G>T (p.Lys262Asn) c.156-367G>T c.570G>T (p.Lys190Asn) c.524G>T (n.524G>T) | |
16 | g.67940441C= | CA2229563357 | LCAT | c.786G= (p.Lys262=) c.156-367G= c.570G= (p.Lys190=) c.524G= (n.524G=) | |
16 | g.67940441C>G | CA396376360 | LCAT | c.786G>C (p.Lys262Asn) c.156-367G>C c.570G>C (p.Lys190Asn) c.524G>C (n.524G>C) | |
16 | g.67940441C>T | CA8120958 | LCAT | c.786G>A (p.Lys262=) c.156-367G>A c.570G>A (p.Lys190=) c.524G>A (n.524G>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.67940442T>A | CA396376361 | LCAT | c.785A>T (p.Lys262Met) c.156-368A>T c.569A>T (p.Lys190Met) c.523A>T (n.523A>T) | |
16 | g.67940442T>C | CA396376362 | LCAT | c.785A>G (p.Lys262Arg) c.156-368A>G c.569A>G (p.Lys190Arg) c.523A>G (n.523A>G) | |
16 | g.67940442T>G | CA396376363 | LCAT | c.785A>C (p.Lys262Thr) c.156-368A>C c.569A>C (p.Lys190Thr) c.523A>C (n.523A>C) | |
16 | g.67940443T>A | CA396376364 | LCAT | c.784A>T (p.Lys262Ter) c.156-369A>T c.568A>T (p.Lys190Ter) c.522A>T (n.522A>T) | |
16 | g.67940443T>C | CA396376366 | LCAT | c.784A>G (p.Lys262Glu) c.156-369A>G c.568A>G (p.Lys190Glu) c.522A>G (n.522A>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.67940443T>G | CA396376365 | LCAT | c.784A>C (p.Lys262Gln) c.156-369A>C c.568A>C (p.Lys190Gln) c.522A>C (n.522A>C) | |
16 | g.67940443T= | CA2229563358 | LCAT | c.784A= (p.Lys262=) c.156-369A= c.568A= (p.Lys190=) c.522A= (n.522A=) | |
16 | g.67940444G>A | CA496384055 | LCAT | c.783C>T (p.Ile261=) c.156-370C>T c.567C>T (p.Ile189=) c.521C>T (n.521C>T) | |
16 | g.67940444G>C | CA396376367 | LCAT | c.783C>G (p.Ile261Met) c.156-370C>G c.567C>G (p.Ile189Met) c.521C>G (n.521C>G) | |
16 | g.67940444G>T | CA496384056 | LCAT | c.783C>A (p.Ile261=) c.156-370C>A c.567C>A (p.Ile189=) c.521C>A (n.521C>A) | |
16 | g.67940445A>C | CA396376368 | LCAT | c.782T>G (p.Ile261Ser) c.156-371T>G c.566T>G (p.Ile189Ser) c.520T>G (n.520T>G) | |
16 | g.67940445A>G | CA396376369 | LCAT | c.782T>C (p.Ile261Thr) c.156-371T>C c.566T>C (p.Ile189Thr) c.520T>C (n.520T>C) | |
16 | g.67940445A>T | CA396376370 | LCAT | c.782T>A (p.Ile261Asn) c.156-371T>A c.566T>A (p.Ile189Asn) c.520T>A (n.520T>A) | |
16 | g.67940446T>A | CA396376373 | LCAT | c.781A>T (p.Ile261Phe) c.156-372A>T c.565A>T (p.Ile189Phe) c.519A>T (n.519A>T) | ClinVar |
16 | g.67940446T>C | CA396376372 | LCAT | c.781A>G (p.Ile261Val) c.156-372A>G c.565A>G (p.Ile189Val) c.519A>G (n.519A>G) | |
16 | g.67940446T>G | CA396376371 | LCAT | c.781A>C (p.Ile261Leu) c.156-372A>C c.565A>C (p.Ile189Leu) c.519A>C (n.519A>C) | |
16 | g.67940447G>A | CA496384057 | LCAT | c.780C>T (p.Ser260=) c.156-373C>T c.564C>T (p.Ser188=) c.518C>T (n.518C>T) | |
16 | g.67940447G>C | CA396376374 | LCAT | c.780C>G (p.Ser260Arg) c.156-373C>G c.564C>G (p.Ser188Arg) c.518C>G (n.518C>G) | |
16 | g.67940447G>T | CA396376375 | LCAT | c.780C>A (p.Ser260Arg) c.156-373C>A c.564C>A (p.Ser188Arg) c.518C>A (n.518C>A) | |
16 | g.67940448C>A | CA396376376 | LCAT | c.779G>T (p.Ser260Ile) c.156-374G>T c.563G>T (p.Ser188Ile) c.517G>T (n.517G>T) | |
16 | g.67940448C= | CA2229563359 | LCAT | c.779G= (p.Ser260=) c.156-374G= c.563G= (p.Ser188=) c.517G= (n.517G=) | |
16 | g.67940448C>G | CA396376377 | LCAT | c.779G>C (p.Ser260Thr) c.156-374G>C c.563G>C (p.Ser188Thr) c.517G>C (n.517G>C) | |
16 | g.67940448C>T | CA8120959 | LCAT | c.779G>A (p.Ser260Asn) c.156-374G>A c.563G>A (p.Ser188Asn) c.517G>A (n.517G>A) | dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.67940449T>A | CA396376378 | LCAT | c.778A>T (p.Ser260Cys) c.156-375A>T c.562A>T (p.Ser188Cys) c.516A>T (n.516A>T) | gnomAD v4 |
16 | g.67940449T>C | CA396376379 | LCAT | c.778A>G (p.Ser260Gly) c.156-375A>G c.562A>G (p.Ser188Gly) c.516A>G (n.516A>G) | |
16 | g.67940449T>G | CA396376380 | LCAT | c.778A>C (p.Ser260Arg) c.156-375A>C c.562A>C (p.Ser188Arg) c.516A>C (n.516A>C) | |
16 | g.67940450G>A | CA8120960 | LCAT | c.777C>T (p.Ser259=) c.156-376C>T c.561C>T (p.Ser187=) c.515C>T (n.515C>T) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.67940450G>C | CA496384058 | LCAT | c.777C>G (p.Ser259=) c.156-376C>G c.561C>G (p.Ser187=) c.515C>G (n.515C>G) | |
16 | g.67940450G= | CA2229563360 | LCAT | c.777C= (p.Ser259=) c.156-376C= c.561C= (p.Ser187=) c.515C= (n.515C=) | |
16 | g.67940450G>T | CA496384059 | LCAT | c.777C>A (p.Ser259=) c.156-376C>A c.561C>A (p.Ser187=) c.515C>A (n.515C>A) | |
16 | g.67940451G>A | CA396376381 | LCAT | c.776C>T (p.Ser259Phe) c.156-377C>T c.560C>T (p.Ser187Phe) c.514C>T (n.514C>T) | |
16 | g.67940451G>C | CA396376382 | LCAT | c.776C>G (p.Ser259Cys) c.156-377C>G c.560C>G (p.Ser187Cys) c.514C>G (n.514C>G) | |
16 | g.67940451G>T | CA396376383 | LCAT | c.776C>A (p.Ser259Tyr) c.156-377C>A c.560C>A (p.Ser187Tyr) c.514C>A (n.514C>A) | |
16 | g.67940452A>C | CA396376384 | LCAT | c.775T>G (p.Ser259Ala) c.156-378T>G c.559T>G (p.Ser187Ala) c.513T>G (n.513T>G) | |
16 | g.67940452A>G | CA396376385 | LCAT | c.775T>C (p.Ser259Pro) c.156-378T>C c.559T>C (p.Ser187Pro) c.513T>C (n.513T>C) | |
16 | g.67940452A>T | CA396376386 | LCAT | c.775T>A (p.Ser259Thr) c.156-378T>A c.559T>A (p.Ser187Thr) c.513T>A (n.513T>A) | |
16 | g.67940453C>A | CA396376387 | LCAT | c.774G>T (p.Met258Ile) c.156-379G>T c.558G>T (p.Met186Ile) c.512G>T (n.512G>T) | |
16 | g.67940453C>G | CA396376389 | LCAT | c.774G>C (p.Met258Ile) c.156-379G>C c.558G>C (p.Met186Ile) c.512G>C (n.512G>C) | |
16 | g.67940453C>T | CA396376388 | LCAT | c.774G>A (p.Met258Ile) c.156-379G>A c.558G>A (p.Met186Ile) c.512G>A (n.512G>A) | |
16 | g.67940454A>C | CA396376390 | LCAT | c.773T>G (p.Met258Arg) c.156-380T>G c.557T>G (p.Met186Arg) c.511T>G (n.511T>G) | |
16 | g.67940454A>G | CA396376391 | LCAT | c.773T>C (p.Met258Thr) c.156-380T>C c.557T>C (p.Met186Thr) c.511T>C (n.511T>C) | gnomAD v2 gnomAD v4 |
16 | g.67940454A>T | CA396376392 | LCAT | c.773T>A (p.Met258Lys) c.156-380T>A c.557T>A (p.Met186Lys) c.511T>A (n.511T>A) | |
16 | g.67940455T>A | CA396376393 | LCAT | c.772A>T (p.Met258Leu) c.156-381A>T c.556A>T (p.Met186Leu) c.510A>T (n.510A>T) | |
16 | g.67940455T>C | CA396376394 | LCAT | c.772A>G (p.Met258Val) c.156-381A>G c.556A>G (p.Met186Val) c.510A>G (n.510A>G) | |
16 | g.67940455T>G | CA396376395 | LCAT | c.772A>C (p.Met258Leu) c.156-381A>C c.556A>C (p.Met186Leu) c.510A>C (n.510A>C) | |
16 | g.67940456G>A | CA496384060 | LCAT | c.771C>T (p.Ile257=) c.156-382C>T c.555C>T (p.Ile185=) c.509C>T (n.509C>T) | dbSNP COSMIC |
16 | g.67940456G>C | CA396376396 | LCAT | c.771C>G (p.Ile257Met) c.156-382C>G c.555C>G (p.Ile185Met) c.509C>G (n.509C>G) | gnomAD v4 |
16 | g.67940456G= | CA2229563361 | LCAT | c.771C= (p.Ile257=) c.156-382C= c.555C= (p.Ile185=) c.509C= (n.509C=) | |
16 | g.67940456G>T | CA496384061 | LCAT | c.771C>A (p.Ile257=) c.156-382C>A c.555C>A (p.Ile185=) c.509C>A (n.509C>A) | |
16 | g.67940457A>C | CA396376397 | LCAT | c.770T>G (p.Ile257Ser) c.156-383T>G c.554T>G (p.Ile185Ser) c.508T>G (n.508T>G) | |
16 | g.67940457A>G | CA396376398 | LCAT | c.770T>C (p.Ile257Thr) c.156-383T>C c.554T>C (p.Ile185Thr) c.508T>C (n.508T>C) | |
16 | g.67940457A>T | CA396376399 | LCAT | c.770T>A (p.Ile257Asn) c.156-383T>A c.554T>A (p.Ile185Asn) c.508T>A (n.508T>A) | |
16 | g.67940458T>A | CA396376402 | LCAT | c.769A>T (p.Ile257Phe) c.156-384A>T c.553A>T (p.Ile185Phe) c.507A>T (n.507A>T) | |
16 | g.67940458T>C | CA396376401 | LCAT | c.769A>G (p.Ile257Val) c.156-384A>G c.553A>G (p.Ile185Val) c.507A>G (n.507A>G) | |
16 | g.67940458T>G | CA396376400 | LCAT | c.769A>C (p.Ile257Leu) c.156-384A>C c.553A>C (p.Ile185Leu) c.507A>C (n.507A>C) | |
16 | g.67940459G>A | CA496384062 | LCAT | c.768C>T (p.Pro256=) c.156-385C>T c.552C>T (p.Pro184=) c.506C>T (n.506C>T) | COSMIC |
16 | g.67940459G>C | CA496384063 | LCAT | c.768C>G (p.Pro256=) c.156-385C>G c.552C>G (p.Pro184=) c.506C>G (n.506C>G) | |
16 | g.67940459G>T | CA496384064 | LCAT | c.768C>A (p.Pro256=) c.156-385C>A c.552C>A (p.Pro184=) c.506C>A (n.506C>A) | |
16 | g.67940460G>A | CA396376403 | LCAT | c.767C>T (p.Pro256Leu) c.156-386C>T c.551C>T (p.Pro184Leu) c.505C>T (n.505C>T) | gnomAD v4 |
16 | g.67940460G>C | CA396376404 | LCAT | c.767C>G (p.Pro256Arg) c.156-386C>G c.551C>G (p.Pro184Arg) c.505C>G (n.505C>G) | |
16 | g.67940460G>T | CA396376405 | LCAT | c.767C>A (p.Pro256His) c.156-386C>A c.551C>A (p.Pro184His) c.505C>A (n.505C>A) | |
16 | g.67940461G>A | CA396376406 | LCAT | c.766C>T (p.Pro256Ser) c.156-387C>T c.550C>T (p.Pro184Ser) c.504C>T (n.504C>T) | COSMIC |
16 | g.67940461G>C | CA396376407 | LCAT | c.766C>G (p.Pro256Ala) c.156-387C>G c.550C>G (p.Pro184Ala) c.504C>G (n.504C>G) | |
16 | g.67940461G>T | CA396376408 | LCAT | c.766C>A (p.Pro256Thr) c.156-387C>A c.550C>A (p.Pro184Thr) c.504C>A (n.504C>A) | |
16 | g.67940462G>A | CA496384066 | LCAT | c.765C>T (p.Ile255=) c.156-388C>T c.549C>T (p.Ile183=) c.503C>T (n.503C>T) | dbSNP gnomAD v3 gnomAD v4 |
16 | g.67940462G>C | CA396376409 | LCAT | c.765C>G (p.Ile255Met) c.156-388C>G c.549C>G (p.Ile183Met) c.503C>G (n.503C>G) | |
16 | g.67940462G= | CA2229563362 | LCAT | c.765C= (p.Ile255=) c.156-388C= c.549C= (p.Ile183=) c.503C= (n.503C=) | |
16 | g.67940462G>T | CA496384065 | LCAT | c.765C>A (p.Ile255=) c.156-388C>A c.549C>A (p.Ile183=) c.503C>A (n.503C>A) | |
16 | g.67940463A>C | CA396376410 | LCAT | c.764T>G (p.Ile255Ser) c.156-389T>G c.548T>G (p.Ile183Ser) c.502T>G (n.502T>G) | |
16 | g.67940463A>G | CA396376411 | LCAT | c.764T>C (p.Ile255Thr) c.156-389T>C c.548T>C (p.Ile183Thr) c.502T>C (n.502T>C) | |
16 | g.67940463A>T | CA396376412 | LCAT | c.764T>A (p.Ile255Asn) c.156-389T>A c.548T>A (p.Ile183Asn) c.502T>A (n.502T>A) | |
16 | g.67940464T>A | CA396376413 | LCAT | c.763A>T (p.Ile255Phe) c.156-390A>T c.547A>T (p.Ile183Phe) c.501A>T (n.501A>T) | |
16 | g.67940464T>C | CA396376414 | LCAT | c.763A>G (p.Ile255Val) c.156-390A>G c.547A>G (p.Ile183Val) c.501A>G (n.501A>G) | |
16 | g.67940464T>G | CA396376415 | LCAT | c.763A>C (p.Ile255Leu) c.156-390A>C c.547A>C (p.Ile183Leu) c.501A>C (n.501A>C) | |
16 | g.67940465G>A | CA496384069 | LCAT | c.762C>T (p.Gly254=) c.156-391C>T c.546C>T (p.Gly182=) c.500C>T (n.500C>T) | |
16 | g.67940465G>C | CA496384068 | LCAT | c.762C>G (p.Gly254=) c.156-391C>G c.546C>G (p.Gly182=) c.500C>G (n.500C>G) | |
16 | g.67940465G>T | CA496384067 | LCAT | c.762C>A (p.Gly254=) c.156-391C>A c.546C>A (p.Gly182=) c.500C>A (n.500C>A) | gnomAD v4 |
16 | g.67940466C>A | CA396376418 | LCAT | c.761G>T (p.Gly254Val) c.156-392G>T c.545G>T (p.Gly182Val) c.499G>T (n.499G>T) | |
16 | g.67940466C>G | CA396376416 | LCAT | c.761G>C (p.Gly254Ala) c.156-392G>C c.545G>C (p.Gly182Ala) c.499G>C (n.499G>C) | |
16 | g.67940466C>T | CA396376417 | LCAT | c.761G>A (p.Gly254Asp) c.156-392G>A c.545G>A (p.Gly182Asp) c.499G>A (n.499G>A) | |
16 | g.67940467C>A | CA396376419 | LCAT | c.760G>T (p.Gly254Cys) c.156-393G>T c.544G>T (p.Gly182Cys) c.498G>T (n.498G>T) | |
16 | g.67940467C= | CA2229563363 | LCAT | c.760G= (p.Gly254=) c.156-393G= c.544G= (p.Gly182=) c.498G= (n.498G=) | |
16 | g.67940467C>G | CA396376420 | LCAT | c.760G>C (p.Gly254Arg) c.156-393G>C c.544G>C (p.Gly182Arg) c.498G>C (n.498G>C) | dbSNP gnomAD v2 gnomAD v4 |
16 | g.67940467C>T | CA396376421 | LCAT | c.760G>A (p.Gly254Ser) c.156-393G>A c.544G>A (p.Gly182Ser) c.498G>A (n.498G>A) | |
16 | g.67940468C>A | CA396376422 | LCAT | c.759G>T (p.Gln253His) c.156-394G>T c.543G>T (p.Gln181His) c.497G>T (n.497G>T) | |
16 | g.67940468C= | CA2229563364 | LCAT | c.759G= (p.Gln253=) c.156-394G= c.543G= (p.Gln181=) c.497G= (n.497G=) | |
16 | g.67940468C>G | CA396376423 | LCAT | c.759G>C (p.Gln253His) c.156-394G>C c.543G>C (p.Gln181His) c.497G>C (n.497G>C) | |
16 | g.67940468C>T | CA8120961 | LCAT | c.759G>A (p.Gln253=) c.156-394G>A c.543G>A (p.Gln181=) c.497G>A (n.497G>A) | dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.67940469del | CA2842798042 | LCAT | c.758del (p.Gln253ArgfsTer11) c.156-395del c.542del (p.Gln181ArgfsTer11) c.496del (n.496del) | |
16 | g.67940469T>A | CA396376424 | LCAT | c.758A>T (p.Gln253Leu) c.156-395A>T c.542A>T (p.Gln181Leu) c.496A>T (n.496A>T) | |
16 | g.67940469T>C | CA396376425 | LCAT | c.758A>G (p.Gln253Arg) c.156-395A>G c.542A>G (p.Gln181Arg) c.496A>G (n.496A>G) | |
16 | g.67940469T>G | CA396376426 | LCAT | c.758A>C (p.Gln253Pro) c.156-395A>C c.542A>C (p.Gln181Pro) c.496A>C (n.496A>C) | |
16 | g.67940470G>A | CA396376427 | LCAT | c.757C>T (p.Gln253Ter) c.156-396C>T c.541C>T (p.Gln181Ter) c.495C>T (n.495C>T) | |
16 | g.67940470G>C | CA396376428 | LCAT | c.757C>G (p.Gln253Glu) c.156-396C>G c.541C>G (p.Gln181Glu) c.495C>G (n.495C>G) | gnomAD v4 |
16 | g.67940470G>T | CA396376429 | LCAT | c.757C>A (p.Gln253Lys) c.156-396C>A c.541C>A (p.Gln181Lys) c.495C>A (n.495C>A) | |
16 | g.67940471G>A | CA496384070 | LCAT | c.756C>T (p.Asn252=) c.156-397C>T c.540C>T (p.Asn180=) c.494C>T (n.494C>T) | |
16 | g.67940471G>C | CA396376430 | LCAT | c.756C>G (p.Asn252Lys) c.156-397C>G c.540C>G (p.Asn180Lys) c.494C>G (n.494C>G) | |
16 | g.67940471G= | CA2229563365 | LCAT | c.756C= (p.Asn252=) c.156-397C= c.540C= (p.Asn180=) c.494C= (n.494C=) | |
16 | g.67940471G>T | CA116417 | LCAT | c.756C>A (p.Asn252Lys) c.156-397C>A c.540C>A (p.Asn180Lys) c.494C>A (n.494C>A) | ClinVar dbSNP gnomAD v4 |
16 | g.67940472T>A | CA396376431 | LCAT | c.755A>T (p.Asn252Ile) c.156-398A>T c.539A>T (p.Asn180Ile) c.493A>T (n.493A>T) | |
16 | g.67940472T>C | CA396376433 | LCAT | c.755A>G (p.Asn252Ser) c.156-398A>G c.539A>G (p.Asn180Ser) c.493A>G (n.493A>G) | |
16 | g.67940472T>G | CA396376432 | LCAT | c.755A>C (p.Asn252Thr) c.156-398A>C c.539A>C (p.Asn180Thr) c.493A>C (n.493A>C) | |
16 | g.67940473T>A | CA396376434 | LCAT | c.754A>T (p.Asn252Tyr) c.156-399A>T c.538A>T (p.Asn180Tyr) c.492A>T (n.492A>T) | |
16 | g.67940473T>C | CA396376436 | LCAT | c.754A>G (p.Asn252Asp) c.156-399A>G c.538A>G (p.Asn180Asp) c.492A>G (n.492A>G) | |
16 | g.67940473T>G | CA396376435 | LCAT | c.754A>C (p.Asn252His) c.156-399A>C c.538A>C (p.Asn180His) c.492A>C (n.492A>C) | |
16 | g.67940474G>A | CA8120962 | LCAT | c.753C>T (p.Asp251=) c.156-400C>T c.537C>T (p.Asp179=) c.491C>T (n.491C>T) | dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.67940474G>C | CA396376437 | LCAT | c.753C>G (p.Asp251Glu) c.156-400C>G c.537C>G (p.Asp179Glu) c.491C>G (n.491C>G) | |
16 | g.67940474G= | CA2229563366 | LCAT | c.753C= (p.Asp251=) c.156-400C= c.537C= (p.Asp179=) c.491C= (n.491C=) | |
16 | g.67940474G>T | CA396376438 | LCAT | c.753C>A (p.Asp251Glu) c.156-400C>A c.537C>A (p.Asp179Glu) c.491C>A (n.491C>A) | |
16 | g.67940475T>A | CA396376439 | LCAT | c.752A>T (p.Asp251Val) c.156-401A>T c.536A>T (p.Asp179Val) c.490A>T (n.490A>T) | |
16 | g.67940475T>C | CA396376440 | LCAT | c.752A>G (p.Asp251Gly) c.156-401A>G c.536A>G (p.Asp179Gly) c.490A>G (n.490A>G) | gnomAD v4 |
16 | g.67940475T>G | CA396376441 | LCAT | c.752A>C (p.Asp251Ala) c.156-401A>C c.536A>C (p.Asp179Ala) c.490A>C (n.490A>C) | |
16 | g.67940476C>A | CA396376442 | LCAT | c.751G>T (p.Asp251Tyr) c.156-402G>T c.535G>T (p.Asp179Tyr) c.489G>T (n.489G>T) | |
16 | g.67940476C= | CA2229563367 | LCAT | c.751G= (p.Asp251=) c.156-402G= c.535G= (p.Asp179=) c.489G= (n.489G=) | |
16 | g.67940476C>G | CA396376443 | LCAT | c.751G>C (p.Asp251His) c.156-402G>C c.535G>C (p.Asp179His) c.489G>C (n.489G>C) | |
16 | g.67940476C>T | CA396376444 | LCAT | c.751G>A (p.Asp251Asn) c.156-402G>A c.535G>A (p.Asp179Asn) c.489G>A (n.489G>A) | dbSNP |
16 | g.67940477A>C | CA496384071 | LCAT | c.750T>G (p.Gly250=) c.156-403T>G c.534T>G (p.Gly178=) c.488T>G (n.488T>G) | |
16 | g.67940477A>G | CA496384072 | LCAT | c.750T>C (p.Gly250=) c.156-403T>C c.534T>C (p.Gly178=) c.488T>C (n.488T>C) | |
16 | g.67940477A>T | CA496384073 | LCAT | c.750T>A (p.Gly250=) c.156-403T>A c.534T>A (p.Gly178=) c.488T>A (n.488T>A) | |
16 | g.67940478C>A | CA396376445 | LCAT | c.749G>T (p.Gly250Val) c.156-404G>T c.533G>T (p.Gly178Val) c.487G>T (n.487G>T) | |
16 | g.67940478C>G | CA396376446 | LCAT | c.749G>C (p.Gly250Ala) c.156-404G>C c.533G>C (p.Gly178Ala) c.487G>C (n.487G>C) | |
16 | g.67940478C>T | CA396376447 | LCAT | c.749G>A (p.Gly250Asp) c.156-404G>A c.533G>A (p.Gly178Asp) c.487G>A (n.487G>A) | |
16 | g.67940479C>A | CA396376450 | LCAT | c.749-1G>T (n.749-1G>T) c.156-405G>T c.533-1G>T (n.533-1G>T) c.487-1G>T (n.487-1G>T) | |
16 | g.67940479C>G | CA396376448 | LCAT | c.749-1G>C (n.749-1G>C) c.156-405G>C c.533-1G>C (n.533-1G>C) c.487-1G>C (n.487-1G>C) | |
16 | g.67940479C>T | CA396376449 | LCAT | c.749-1G>A (n.749-1G>A) c.156-405G>A c.533-1G>A (n.533-1G>A) c.487-1G>A (n.487-1G>A) | |
16 | g.67940480T>A | CA396376451 | LCAT | c.749-2A>T (n.749-2A>T) c.156-406A>T c.533-2A>T (n.533-2A>T) c.487-2A>T (n.487-2A>T) | |
16 | g.67940480T>C | CA396376452 | LCAT | c.749-2A>G (n.749-2A>G) c.156-406A>G c.533-2A>G (n.533-2A>G) c.487-2A>G (n.487-2A>G) | dbSNP gnomAD v3 gnomAD v4 |
16 | g.67940480T>G | CA396376453 | LCAT | c.749-2A>C (n.749-2A>C) c.156-406A>C c.533-2A>C (n.533-2A>C) c.487-2A>C (n.487-2A>C) | |
16 | g.67940484G= | CA2229563368 | LCAT | c.749-6C= (n.749-6C=) c.156-410C= c.533-6C= (n.533-6C=) c.487-6C= (n.487-6C=) | |
16 | g.67940484G>T | CA623122293 | LCAT | c.749-6C>A (n.749-6C>A) c.156-410C>A c.533-6C>A (n.533-6C>A) c.487-6C>A (n.487-6C>A) | dbSNP gnomAD v2 gnomAD v4 |
16 | g.67940485A= | CA2229563369 | LCAT | c.749-7T= (n.749-7T=) c.156-411T= c.533-7T= (n.533-7T=) c.487-7T= (n.487-7T=) | |
16 | g.67940485A>G | CA2229563370 | LCAT | c.749-7T>C (n.749-7T>C) c.156-411T>C c.533-7T>C (n.533-7T>C) c.487-7T>C (n.487-7T>C) | dbSNP gnomAD v4 |
16 | g.67940486T>A | CA2576033453 | LCAT | c.749-8A>T (n.749-8A>T) c.156-412A>T c.533-8A>T (n.533-8A>T) c.487-8A>T (n.487-8A>T) | gnomAD v4 |
16 | g.67940486T>C | CA2505093749 | LCAT | c.749-8A>G (n.749-8A>G) c.156-412A>G c.533-8A>G (n.533-8A>G) c.487-8A>G (n.487-8A>G) | gnomAD v4 |
16 | g.67940488del | CA2633851075 | LCAT | c.749-10del (n.749-10del) c.156-414del c.533-10del (n.533-10del) c.487-10del (n.487-10del) | gnomAD v4 |
16 | g.67940488T>C | CA283161104 | LCAT | c.749-10A>G (n.749-10A>G) c.156-414A>G c.533-10A>G (n.533-10A>G) c.487-10A>G (n.487-10A>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.67940488T= | CA2229563371 | LCAT | c.749-10A= (n.749-10A=) c.156-414A= c.533-10A= (n.533-10A=) c.487-10A= (n.487-10A=) | |
16 | g.67940489G>A | CA2510296598 | LCAT | c.749-11C>T (n.749-11C>T) c.156-415C>T c.533-11C>T (n.533-11C>T) c.487-11C>T (n.487-11C>T) | |
16 | g.67940490G>A | CA8120963 | LCAT | c.749-12C>T (n.749-12C>T) c.156-416C>T c.533-12C>T (n.533-12C>T) c.487-12C>T (n.487-12C>T) | dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.67940490G>C | CA2633851080 | LCAT | c.749-12C>G (n.749-12C>G) c.156-416C>G c.533-12C>G (n.533-12C>G) c.487-12C>G (n.487-12C>G) | gnomAD v4 |
16 | g.67940490G= | CA2229563372 | LCAT | c.749-12C= (n.749-12C=) c.156-416C= c.533-12C= (n.533-12C=) c.487-12C= (n.487-12C=) | |
16 | g.67940491A= | CA2229563373 | LCAT | c.749-13T= (n.749-13T=) c.156-417T= c.533-13T= (n.533-13T=) c.487-13T= (n.487-13T=) | |
16 | g.67940491A>C | CA656474646 | LCAT | c.749-13T>G (n.749-13T>G) c.156-417T>G c.533-13T>G (n.533-13T>G) c.487-13T>G (n.487-13T>G) | COSMIC |
16 | g.67940491A>T | CA723097944 | LCAT | c.749-13T>A (n.749-13T>A) c.156-417T>A c.533-13T>A (n.533-13T>A) c.487-13T>A (n.487-13T>A) | dbSNP gnomAD v4 |
16 | g.67940492G>A | CA8120964 | LCAT | c.749-14C>T (n.749-14C>T) c.156-418C>T c.533-14C>T (n.533-14C>T) c.487-14C>T (n.487-14C>T) | dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.67940492G= | CA2229563374 | LCAT | c.749-14C= (n.749-14C=) c.156-418C= c.533-14C= (n.533-14C=) c.487-14C= (n.487-14C=) | |
16 | g.67940493C= | CA2229563375 | LCAT | c.749-15G= (n.749-15G=) c.156-419G= c.533-15G= (n.533-15G=) c.487-15G= (n.487-15G=) | |
16 | g.67940493C>G | CA623122294 | LCAT | c.749-15G>C (n.749-15G>C) c.156-419G>C c.533-15G>C (n.533-15G>C) c.487-15G>C (n.487-15G>C) | dbSNP gnomAD v2 gnomAD v4 |
16 | g.67940495A>T | CA2633851129 | LCAT | c.749-17T>A (n.749-17T>A) c.156-421T>A c.533-17T>A (n.533-17T>A) c.487-17T>A (n.487-17T>A) | gnomAD v4 |