UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 11 | g.44275400T>A | CA380182238 | ALX4 | c.725A>T (p.Tyr242Phe) c.203A>T (p.Tyr68Phe) | |
| 11 | g.44275400T>C | CA380182237 | ALX4 | c.725A>G (p.Tyr242Cys) c.203A>G (p.Tyr68Cys) | |
| 11 | g.44275400T>G | CA380182236 | ALX4 | c.725A>C (p.Tyr242Ser) c.203A>C (p.Tyr68Ser) | |
| 11 | g.44275401A>C | CA380182239 | ALX4 | c.724T>G (p.Tyr242Asp) c.202T>G (p.Tyr68Asp) | |
| 11 | g.44275401A>G | CA380182240 | ALX4 | c.724T>C (p.Tyr242His) c.202T>C (p.Tyr68His) | gnomAD v4 |
| 11 | g.44275401A>T | CA380182241 | ALX4 | c.724T>A (p.Tyr242Asn) c.202T>A (p.Tyr68Asn) | |
| 11 | g.44275402C>A | CA473833890 | ALX4 | c.723G>T (p.Val241=) c.201G>T (p.Val67=) | |
| 11 | g.44275402C>G | CA473833891 | ALX4 | c.723G>C (p.Val241=) c.201G>C (p.Val67=) | |
| 11 | g.44275402C>T | CA473833892 | ALX4 | c.723G>A (p.Val241=) c.201G>A (p.Val67=) | |
| 11 | g.44275403A>C | CA380182242 | ALX4 | c.722T>G (p.Val241Gly) c.200T>G (p.Val67Gly) | |
| 11 | g.44275403A>G | CA380182243 | ALX4 | c.722T>C (p.Val241Ala) c.200T>C (p.Val67Ala) | |
| 11 | g.44275403A>T | CA380182244 | ALX4 | c.722T>A (p.Val241Glu) c.200T>A (p.Val67Glu) | |
| 11 | g.44275404C>A | CA5955670 | ALX4 | c.721G>T (p.Val241Leu) c.199G>T (p.Val67Leu) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.44275404C= | CA1967928957 | ALX4 | c.721G= (p.Val241=) c.199G= (p.Val67=) | |
| 11 | g.44275404C>G | CA380182245 | ALX4 | c.721G>C (p.Val241Leu) c.199G>C (p.Val67Leu) | |
| 11 | g.44275404C>T | CA5955671 | ALX4 | c.721G>A (p.Val241Met) c.199G>A (p.Val67Met) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.44275405G>A | CA5955672 | ALX4 | c.720C>T (p.Asp240=) c.198C>T (p.Asp66=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 11 | g.44275405G>C | CA380182246 | ALX4 | c.720C>G (p.Asp240Glu) c.198C>G (p.Asp66Glu) | |
| 11 | g.44275405G= | CA1967928959 | ALX4 | c.720C= (p.Asp240=) c.198C= (p.Asp66=) | |
| 11 | g.44275405G>T | CA380182247 | ALX4 | c.720C>A (p.Asp240Glu) c.198C>A (p.Asp66Glu) | |
| 11 | g.44275406T>A | CA380182250 | ALX4 | c.719A>T (p.Asp240Val) c.197A>T (p.Asp66Val) | |
| 11 | g.44275406T>C | CA380182249 | ALX4 | c.719A>G (p.Asp240Gly) c.197A>G (p.Asp66Gly) | |
| 11 | g.44275406T>G | CA380182248 | ALX4 | c.719A>C (p.Asp240Ala) c.197A>C (p.Asp66Ala) | |
| 11 | g.44275407C>A | CA380182251 | ALX4 | c.718G>T (p.Asp240Tyr) c.196G>T (p.Asp66Tyr) | |
| 11 | g.44275407C>G | CA380182253 | ALX4 | c.718G>C (p.Asp240His) c.196G>C (p.Asp66His) | |
| 11 | g.44275407C>T | CA380182252 | ALX4 | c.718G>A (p.Asp240Asn) c.196G>A (p.Asp66Asn) | |
| 11 | g.44275408T>A | CA473833895 | ALX4 | c.717A>T (p.Pro239=) c.195A>T (p.Pro65=) | gnomAD v4 |
| 11 | g.44275408T>C | CA473833896 | ALX4 | c.717A>G (p.Pro239=) c.195A>G (p.Pro65=) | dbSNP gnomAD v3 gnomAD v4 |
| 11 | g.44275408T>G | CA473833897 | ALX4 | c.717A>C (p.Pro239=) c.195A>C (p.Pro65=) | |
| 11 | g.44275408T= | CA1967928961 | ALX4 | c.717A= (p.Pro239=) c.195A= (p.Pro65=) | |
| 11 | g.44275409G>A | CA380182254 | ALX4 | c.716C>T (p.Pro239Leu) c.194C>T (p.Pro65Leu) | |
| 11 | g.44275409G>C | CA380182255 | ALX4 | c.716C>G (p.Pro239Arg) c.194C>G (p.Pro65Arg) | |
| 11 | g.44275409G>T | CA380182256 | ALX4 | c.716C>A (p.Pro239Gln) c.194C>A (p.Pro65Gln) | |
| 11 | g.44275410G>A | CA380182257 | ALX4 | c.715C>T (p.Pro239Ser) c.193C>T (p.Pro65Ser) | |
| 11 | g.44275410G>C | CA380182258 | ALX4 | c.715C>G (p.Pro239Ala) c.193C>G (p.Pro65Ala) | |
| 11 | g.44275410G>T | CA380182259 | ALX4 | c.715C>A (p.Pro239Thr) c.193C>A (p.Pro65Thr) | |
| 11 | g.44275411G>A | CA5955673 | ALX4 | c.714C>T (p.Tyr238=) c.192C>T (p.Tyr64=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 11 | g.44275411G>C | CA380182260 | ALX4 | c.714C>G (p.Tyr238Ter) c.192C>G (p.Tyr64Ter) | |
| 11 | g.44275411G= | CA1967928964 | ALX4 | c.714C= (p.Tyr238=) c.192C= (p.Tyr64=) | |
| 11 | g.44275411G>T | CA380182261 | ALX4 | c.714C>A (p.Tyr238Ter) c.192C>A (p.Tyr64Ter) | |
| 11 | g.44275412T>A | CA380182262 | ALX4 | c.713A>T (p.Tyr238Phe) c.191A>T (p.Tyr64Phe) | |
| 11 | g.44275412T>C | CA380182263 | ALX4 | c.713A>G (p.Tyr238Cys) c.191A>G (p.Tyr64Cys) | |
| 11 | g.44275412T>G | CA380182264 | ALX4 | c.713A>C (p.Tyr238Ser) c.191A>C (p.Tyr64Ser) | |
| 11 | g.44275413A>C | CA380182267 | ALX4 | c.712T>G (p.Tyr238Asp) c.190T>G (p.Tyr64Asp) | |
| 11 | g.44275413A>G | CA380182265 | ALX4 | c.712T>C (p.Tyr238His) c.190T>C (p.Tyr64His) | |
| 11 | g.44275413A>T | CA380182266 | ALX4 | c.712T>A (p.Tyr238Asn) c.190T>A (p.Tyr64Asn) | |
| 11 | g.44275414G>A | CA473833902 | ALX4 | c.711C>T (p.His237=) c.189C>T (p.His63=) | |
| 11 | g.44275414G>C | CA380182268 | ALX4 | c.711C>G (p.His237Gln) c.189C>G (p.His63Gln) | |
| 11 | g.44275414G>T | CA380182269 | ALX4 | c.711C>A (p.His237Gln) c.189C>A (p.His63Gln) | |
| 11 | g.44275415T>A | CA380182270 | ALX4 | c.710A>T (p.His237Leu) c.188A>T (p.His63Leu) | |
| 11 | g.44275415T>C | CA380182271 | ALX4 | c.710A>G (p.His237Arg) c.188A>G (p.His63Arg) | gnomAD v4 |
| 11 | g.44275415T>G | CA380182272 | ALX4 | c.710A>C (p.His237Pro) c.188A>C (p.His63Pro) | |
| 11 | g.44275416G>A | CA380182273 | ALX4 | c.709C>T (p.His237Tyr) c.187C>T (p.His63Tyr) | |
| 11 | g.44275416G>C | CA380182274 | ALX4 | c.709C>G (p.His237Asp) c.187C>G (p.His63Asp) | |
| 11 | g.44275416G>T | CA380182275 | ALX4 | c.709C>A (p.His237Asn) c.187C>A (p.His63Asn) | gnomAD v4 |
| 11 | g.44275417G>A | CA473833909 | ALX4 | c.708C>T (p.Thr236=) c.186C>T (p.Thr62=) | |
| 11 | g.44275417G>C | CA473833905 | ALX4 | c.708C>G (p.Thr236=) c.186C>G (p.Thr62=) | COSMIC |
| 11 | g.44275417G>T | CA473833907 | ALX4 | c.708C>A (p.Thr236=) c.186C>A (p.Thr62=) | |
| 11 | g.44275418G>A | CA380182276 | ALX4 | c.707C>T (p.Thr236Ile) c.185C>T (p.Thr62Ile) | |
| 11 | g.44275418G>C | CA380182277 | ALX4 | c.707C>G (p.Thr236Ser) c.185C>G (p.Thr62Ser) | |
| 11 | g.44275418G= | CA1967928966 | ALX4 | c.707C= (p.Thr236=) c.185C= (p.Thr62=) | |
| 11 | g.44275418G>T | CA380182278 | ALX4 | c.707C>A (p.Thr236Asn) c.185C>A (p.Thr62Asn) | dbSNP gnomAD v4 |
| 11 | g.44275419T>A | CA380182281 | ALX4 | c.706A>T (p.Thr236Ser) c.184A>T (p.Thr62Ser) | |
| 11 | g.44275419T>C | CA380182280 | ALX4 | c.706A>G (p.Thr236Ala) c.184A>G (p.Thr62Ala) | |
| 11 | g.44275419T>G | CA380182279 | ALX4 | c.706A>C (p.Thr236Pro) c.184A>C (p.Thr62Pro) | |
| 11 | g.44275420C>A | CA380182282 | ALX4 | c.705G>T (p.Lys235Asn) c.183G>T (p.Lys61Asn) | |
| 11 | g.44275420C>G | CA380182283 | ALX4 | c.705G>C (p.Lys235Asn) c.183G>C (p.Lys61Asn) | |
| 11 | g.44275420C>T | CA473833913 | ALX4 | c.705G>A (p.Lys235=) c.183G>A (p.Lys61=) | |
| 11 | g.44275421T>A | CA380182284 | ALX4 | c.704A>T (p.Lys235Met) c.182A>T (p.Lys61Met) | |
| 11 | g.44275421T>C | CA380182285 | ALX4 | c.704A>G (p.Lys235Arg) c.182A>G (p.Lys61Arg) | |
| 11 | g.44275421T>G | CA380182286 | ALX4 | c.704A>C (p.Lys235Thr) c.182A>C (p.Lys61Thr) | |
| 11 | g.44275422T>A | CA380182287 | ALX4 | c.703A>T (p.Lys235Ter) c.181A>T (p.Lys61Ter) | |
| 11 | g.44275422T>C | CA380182288 | ALX4 | c.703A>G (p.Lys235Glu) c.181A>G (p.Lys61Glu) | |
| 11 | g.44275422T>G | CA380182289 | ALX4 | c.703A>C (p.Lys235Gln) c.181A>C (p.Lys61Gln) | |
| 11 | g.44275423C>A | CA380182290 | ALX4 | c.702G>T (p.Gln234His) c.180G>T (p.Gln60His) | |
| 11 | g.44275423C>G | CA380182291 | ALX4 | c.702G>C (p.Gln234His) c.180G>C (p.Gln60His) | gnomAD v4 |
| 11 | g.44275423C>T | CA473833917 | ALX4 | c.702G>A (p.Gln234=) c.180G>A (p.Gln60=) | gnomAD v4 |
| 11 | g.44275424T>A | CA380182292 | ALX4 | c.701A>T (p.Gln234Leu) c.179A>T (p.Gln60Leu) | |
| 11 | g.44275424T>C | CA380182293 | ALX4 | c.701A>G (p.Gln234Arg) c.179A>G (p.Gln60Arg) | dbSNP gnomAD v3 gnomAD v4 |
| 11 | g.44275424T>G | CA5955674 | ALX4 | c.701A>C (p.Gln234Pro) c.179A>C (p.Gln60Pro) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 11 | g.44275424T= | CA1967928970 | ALX4 | c.701A= (p.Gln234=) c.179A= (p.Gln60=) | |
| 11 | g.44275425G>A | CA380182296 | ALX4 | c.700C>T (p.Gln234Ter) c.178C>T (p.Gln60Ter) | COSMIC |
| 11 | g.44275425G>C | CA380182294 | ALX4 | c.700C>G (p.Gln234Glu) c.178C>G (p.Gln60Glu) | |
| 11 | g.44275425G>T | CA380182295 | ALX4 | c.700C>A (p.Gln234Lys) c.178C>A (p.Gln60Lys) | |
| 11 | g.44275426G>A | CA473833919 | ALX4 | c.699C>T (p.Phe233=) c.177C>T (p.Phe59=) | |
| 11 | g.44275426G>C | CA380182297 | ALX4 | c.699C>G (p.Phe233Leu) c.177C>G (p.Phe59Leu) | |
| 11 | g.44275426G= | CA1967928973 | ALX4 | c.699C= (p.Phe233=) c.177C= (p.Phe59=) | |
| 11 | g.44275426G>T | CA380182298 | ALX4 | c.699C>A (p.Phe233Leu) c.177C>A (p.Phe59Leu) | |
| 11 | g.44275427A>C | CA380182299 | ALX4 | c.698T>G (p.Phe233Cys) c.176T>G (p.Phe59Cys) | |
| 11 | g.44275427A>G | CA380182300 | ALX4 | c.698T>C (p.Phe233Ser) c.176T>C (p.Phe59Ser) | |
| 11 | g.44275427A>T | CA380182301 | ALX4 | c.698T>A (p.Phe233Tyr) c.176T>A (p.Phe59Tyr) | |
| 11 | g.44275428dup | CA1967928975 | ALX4 | c.698dup (p.Gln234ProfsTer22) c.176dup (p.Gln60ProfsTer22) | dbSNP |
| 11 | g.44275428A>C | CA380182302 | ALX4 | c.697T>G (p.Phe233Val) c.175T>G (p.Phe59Val) | |
| 11 | g.44275428A>G | CA380182303 | ALX4 | c.697T>C (p.Phe233Leu) c.175T>C (p.Phe59Leu) | |
| 11 | g.44275428A>T | CA380182304 | ALX4 | c.697T>A (p.Phe233Ile) c.175T>A (p.Phe59Ile) | |
| 11 | g.44275429G>A | CA473833921 | ALX4 | c.696C>T (p.Val232=) c.174C>T (p.Val58=) | |
| 11 | g.44275429G>C | CA473833922 | ALX4 | c.696C>G (p.Val232=) c.174C>G (p.Val58=) | |
| 11 | g.44275429G>T | CA473833923 | ALX4 | c.696C>A (p.Val232=) c.174C>A (p.Val58=) | |
| 11 | g.44275430A= | CA1967928979 | ALX4 | c.695T= (p.Val232=) c.173T= (p.Val58=) | |
| 11 | g.44275430A>C | CA380182305 | ALX4 | c.695T>G (p.Val232Gly) c.173T>G (p.Val58Gly) | dbSNP |
| 11 | g.44275430A>G | CA380182306 | ALX4 | c.695T>C (p.Val232Ala) c.173T>C (p.Val58Ala) | |
| 11 | g.44275430A>T | CA380182307 | ALX4 | c.695T>A (p.Val232Asp) c.173T>A (p.Val58Asp) | |
| 11 | g.44275431C>A | CA380182310 | ALX4 | c.694G>T (p.Val232Phe) c.172G>T (p.Val58Phe) | |
| 11 | g.44275431C>G | CA380182309 | ALX4 | c.694G>C (p.Val232Leu) c.172G>C (p.Val58Leu) | |
| 11 | g.44275431C>T | CA380182308 | ALX4 | c.694G>A (p.Val232Ile) c.172G>A (p.Val58Ile) | |
| 11 | g.44275432C>A | CA380182311 | ALX4 | c.693G>T (p.Lys231Asn) c.171G>T (p.Lys57Asn) | |
| 11 | g.44275432C>G | CA380182312 | ALX4 | c.693G>C (p.Lys231Asn) c.171G>C (p.Lys57Asn) | |
| 11 | g.44275432C>T | CA473833925 | ALX4 | c.693G>A (p.Lys231=) c.171G>A (p.Lys57=) | gnomAD v4 |
| 11 | g.44275433T>A | CA380182313 | ALX4 | c.692A>T (p.Lys231Met) c.170A>T (p.Lys57Met) | |
| 11 | g.44275433T>C | CA380182315 | ALX4 | c.692A>G (p.Lys231Arg) c.170A>G (p.Lys57Arg) | dbSNP |
| 11 | g.44275433T>G | CA380182314 | ALX4 | c.692A>C (p.Lys231Thr) c.170A>C (p.Lys57Thr) | |
| 11 | g.44275433T= | CA1967928981 | ALX4 | c.692A= (p.Lys231=) c.170A= (p.Lys57=) | |
| 11 | g.44275434T>A | CA380182316 | ALX4 | c.691A>T (p.Lys231Ter) c.169A>T (p.Lys57Ter) | |
| 11 | g.44275434T>C | CA380182318 | ALX4 | c.691A>G (p.Lys231Glu) c.169A>G (p.Lys57Glu) | gnomAD v4 |
| 11 | g.44275434T>G | CA380182317 | ALX4 | c.691A>C (p.Lys231Gln) c.169A>C (p.Lys57Gln) | |
| 11 | g.44275435C>A | CA380182319 | ALX4 | c.690G>T (p.Glu230Asp) c.168G>T (p.Glu56Asp) | |
| 11 | g.44275435C= | CA1967928983 | ALX4 | c.690G= (p.Glu230=) c.168G= (p.Glu56=) | |
| 11 | g.44275435C>G | CA380182320 | ALX4 | c.690G>C (p.Glu230Asp) c.168G>C (p.Glu56Asp) | |
| 11 | g.44275435C>T | CA221497500 | ALX4 | c.690G>A (p.Glu230=) c.168G>A (p.Glu56=) | dbSNP |
| 11 | g.44275436T>A | CA380182321 | ALX4 | c.689A>T (p.Glu230Val) c.167A>T (p.Glu56Val) | |
| 11 | g.44275436T>C | CA380182322 | ALX4 | c.689A>G (p.Glu230Gly) c.167A>G (p.Glu56Gly) | |
| 11 | g.44275436T>G | CA380182323 | ALX4 | c.689A>C (p.Glu230Ala) c.167A>C (p.Glu56Ala) | |
| 11 | g.44275437C>A | CA380182324 | ALX4 | c.688G>T (p.Glu230Ter) c.166G>T (p.Glu56Ter) | |
| 11 | g.44275437C>G | CA380182325 | ALX4 | c.688G>C (p.Glu230Gln) c.166G>C (p.Glu56Gln) | |
| 11 | g.44275437C>T | CA380182326 | ALX4 | c.688G>A (p.Glu230Lys) c.166G>A (p.Glu56Lys) | |
| 11 | g.44275438C>A | CA474035508 | ALX4 | c.687G>T (p.Leu229=) c.165G>T (p.Leu55=) | |
| 11 | g.44275438C>G | CA474035510 | ALX4 | c.687G>C (p.Leu229=) c.165G>C (p.Leu55=) | |
| 11 | g.44275438C>T | CA474035511 | ALX4 | c.687G>A (p.Leu229=) c.165G>A (p.Leu55=) | gnomAD v4 |
| 11 | g.44275439A>C | CA380182327 | ALX4 | c.686T>G (p.Leu229Arg) c.164T>G (p.Leu55Arg) | |
| 11 | g.44275439A>G | CA380182328 | ALX4 | c.686T>C (p.Leu229Pro) c.164T>C (p.Leu55Pro) | |
| 11 | g.44275439A>T | CA380182329 | ALX4 | c.686T>A (p.Leu229Gln) c.164T>A (p.Leu55Gln) | |
| 11 | g.44275440G>A | CA474035519 | ALX4 | c.685C>T (p.Leu229=) c.163C>T (p.Leu55=) | |
| 11 | g.44275440G>C | CA380182330 | ALX4 | c.685C>G (p.Leu229Val) c.163C>G (p.Leu55Val) | |
| 11 | g.44275440G= | CA1967928986 | ALX4 | c.685C= (p.Leu229=) c.163C= (p.Leu55=) | |
| 11 | g.44275440G>T | CA5955675 | ALX4 | c.685C>A (p.Leu229Met) c.163C>A (p.Leu55Met) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 11 | g.44275441C>A | CA380182332 | ALX4 | c.684G>T (p.Glu228Asp) c.162G>T (p.Glu54Asp) | |
| 11 | g.44275441C= | CA1967928992 | ALX4 | c.684G= (p.Glu228=) c.162G= (p.Glu54=) | |
| 11 | g.44275441C>G | CA380182331 | ALX4 | c.684G>C (p.Glu228Asp) c.162G>C (p.Glu54Asp) | |
| 11 | g.44275441C>T | CA5955676 | ALX4 | c.684G>A (p.Glu228=) c.162G>A (p.Glu54=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 11 | g.44275442T>A | CA380182333 | ALX4 | c.683A>T (p.Glu228Val) c.161A>T (p.Glu54Val) | |
| 11 | g.44275442T>C | CA380182334 | ALX4 | c.683A>G (p.Glu228Gly) c.161A>G (p.Glu54Gly) | |
| 11 | g.44275442T>G | CA380182335 | ALX4 | c.683A>C (p.Glu228Ala) c.161A>C (p.Glu54Ala) | |
| 11 | g.44275443C>A | CA380182336 | ALX4 | c.682G>T (p.Glu228Ter) c.160G>T (p.Glu54Ter) | gnomAD v4 |
| 11 | g.44275443C= | CA1967928997 | ALX4 | c.682G= (p.Glu228=) c.160G= (p.Glu54=) | |
| 11 | g.44275443C>G | CA380182337 | ALX4 | c.682G>C (p.Glu228Gln) c.160G>C (p.Glu54Gln) | gnomAD v4 |
| 11 | g.44275443C>T | CA221497510 | ALX4 | c.682G>A (p.Glu228Lys) c.160G>A (p.Glu54Lys) | dbSNP gnomAD v3 gnomAD v4 COSMIC |
| 11 | g.44275444C>A | CA380182338 | ALX4 | c.681G>T (p.Glu227Asp) c.159G>T (p.Glu53Asp) | COSMIC |
| 11 | g.44275444C>G | CA380182339 | ALX4 | c.681G>C (p.Glu227Asp) c.159G>C (p.Glu53Asp) | |
| 11 | g.44275444C>T | CA474035529 | ALX4 | c.681G>A (p.Glu227=) c.159G>A (p.Glu53=) | |
| 11 | g.44275445T>A | CA380182340 | ALX4 | c.680A>T (p.Glu227Val) c.158A>T (p.Glu53Val) | |
| 11 | g.44275445T>C | CA5955677 | ALX4 | c.680A>G (p.Glu227Gly) c.158A>G (p.Glu53Gly) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 11 | g.44275445T>G | CA380182341 | ALX4 | c.680A>C (p.Glu227Ala) c.158A>C (p.Glu53Ala) | |
| 11 | g.44275445T= | CA1967928999 | ALX4 | c.680A= (p.Glu227=) c.158A= (p.Glu53=) | |
| 11 | g.44275446C>A | CA380182342 | ALX4 | c.679G>T (p.Glu227Ter) c.157G>T (p.Glu53Ter) | |
| 11 | g.44275446C= | CA1967929003 | ALX4 | c.679G= (p.Glu227=) c.157G= (p.Glu53=) | |
| 11 | g.44275446C>G | CA380182343 | ALX4 | c.679G>C (p.Glu227Gln) c.157G>C (p.Glu53Gln) | |
| 11 | g.44275446C>T | CA5955678 | ALX4 | c.679G>A (p.Glu227Lys) c.157G>A (p.Glu53Lys) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.44275447C>A | CA474035544 | ALX4 | c.678G>T (p.Leu226=) c.156G>T (p.Leu52=) | |
| 11 | g.44275447C>G | CA474035543 | ALX4 | c.678G>C (p.Leu226=) c.156G>C (p.Leu52=) | |
| 11 | g.44275447C>T | CA474035542 | ALX4 | c.678G>A (p.Leu226=) c.156G>A (p.Leu52=) | |
| 11 | g.44275448A>C | CA380182344 | ALX4 | c.677T>G (p.Leu226Arg) c.155T>G (p.Leu52Arg) | |
| 11 | g.44275448A>G | CA380182345 | ALX4 | c.677T>C (p.Leu226Pro) c.155T>C (p.Leu52Pro) | |
| 11 | g.44275448A>T | CA380182346 | ALX4 | c.677T>A (p.Leu226Gln) c.155T>A (p.Leu52Gln) | |
| 11 | g.44275449G>A | CA5955679 | ALX4 | c.676C>T (p.Leu226=) c.154C>T (p.Leu52=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.44275449G>C | CA380182347 | ALX4 | c.676C>G (p.Leu226Val) c.154C>G (p.Leu52Val) | |
| 11 | g.44275449G= | CA1967929005 | ALX4 | c.676C= (p.Leu226=) c.154C= (p.Leu52=) | |
| 11 | g.44275449G>T | CA380182348 | ALX4 | c.676C>A (p.Leu226Met) c.154C>A (p.Leu52Met) | |
| 11 | g.44275450C>A | CA380182349 | ALX4 | c.675G>T (p.Gln225His) c.153G>T (p.Gln51His) | |
| 11 | g.44275450C>G | CA380182350 | ALX4 | c.675G>C (p.Gln225His) c.153G>C (p.Gln51His) | |
| 11 | g.44275450C>T | CA474035551 | ALX4 | c.675G>A (p.Gln225=) c.153G>A (p.Gln51=) | |
| 11 | g.44275451T>A | CA380182351 | ALX4 | c.674A>T (p.Gln225Leu) c.152A>T (p.Gln51Leu) | |
| 11 | g.44275451T>C | CA380182352 | ALX4 | c.674A>G (p.Gln225Arg) c.152A>G (p.Gln51Arg) | |
| 11 | g.44275451T>G | CA380182353 | ALX4 | c.674A>C (p.Gln225Pro) c.152A>C (p.Gln51Pro) | |
| 11 | g.44275452G>A | CA380182355 | ALX4 | c.673C>T (p.Gln225Ter) c.151C>T (p.Gln51Ter) | |
| 11 | g.44275452G>C | CA170723 | ALX4 | c.673C>G (p.Gln225Glu) c.151C>G (p.Gln51Glu) | ClinVar dbSNP |
| 11 | g.44275452G= | CA1967929013 | ALX4 | c.673C= (p.Gln225=) c.151C= (p.Gln51=) | |
| 11 | g.44275452G>T | CA380182354 | ALX4 | c.673C>A (p.Gln225Lys) c.151C>A (p.Gln51Lys) | |
| 11 | g.44275453G>A | CA474035558 | ALX4 | c.672C>T (p.Tyr224=) c.150C>T (p.Tyr50=) | dbSNP gnomAD v4 |
| 11 | g.44275453G>C | CA380182356 | ALX4 | c.672C>G (p.Tyr224Ter) c.150C>G (p.Tyr50Ter) | |
| 11 | g.44275453G= | CA1967929020 | ALX4 | c.672C= (p.Tyr224=) c.150C= (p.Tyr50=) | |
| 11 | g.44275453G>T | CA380182357 | ALX4 | c.672C>A (p.Tyr224Ter) c.150C>A (p.Tyr50Ter) | |
| 11 | g.44275454T>A | CA380182358 | ALX4 | c.671A>T (p.Tyr224Phe) c.149A>T (p.Tyr50Phe) | |
| 11 | g.44275454T>C | CA380182359 | ALX4 | c.671A>G (p.Tyr224Cys) c.149A>G (p.Tyr50Cys) | gnomAD v4 |
| 11 | g.44275454T>G | CA380182360 | ALX4 | c.671A>C (p.Tyr224Ser) c.149A>C (p.Tyr50Ser) | |
| 11 | g.44275455A>C | CA380182363 | ALX4 | c.670T>G (p.Tyr224Asp) c.148T>G (p.Tyr50Asp) | |
| 11 | g.44275455A>G | CA380182361 | ALX4 | c.670T>C (p.Tyr224His) c.148T>C (p.Tyr50His) | |
| 11 | g.44275455A>T | CA380182362 | ALX4 | c.670T>A (p.Tyr224Asn) c.148T>A (p.Tyr50Asn) | |
| 11 | g.44275456G>A | CA474035565 | ALX4 | c.669C>T (p.Ser223=) c.147C>T (p.Ser49=) | |
| 11 | g.44275456G>C | CA380182364 | ALX4 | c.669C>G (p.Ser223Arg) c.147C>G (p.Ser49Arg) | |
| 11 | g.44275456G>T | CA380182365 | ALX4 | c.669C>A (p.Ser223Arg) c.147C>A (p.Ser49Arg) | gnomAD v4 |
| 11 | g.44275457C>A | CA380182366 | ALX4 | c.668G>T (p.Ser223Ile) c.146G>T (p.Ser49Ile) | |
| 11 | g.44275457C>G | CA380182367 | ALX4 | c.668G>C (p.Ser223Thr) c.146G>C (p.Ser49Thr) | |
| 11 | g.44275457C>T | CA380182368 | ALX4 | c.668G>A (p.Ser223Asn) c.146G>A (p.Ser49Asn) | |
| 11 | g.44275458T>A | CA380182371 | ALX4 | c.667A>T (p.Ser223Cys) c.145A>T (p.Ser49Cys) | |
| 11 | g.44275458T>C | CA380182370 | ALX4 | c.667A>G (p.Ser223Gly) c.145A>G (p.Ser49Gly) | |
| 11 | g.44275458T>G | CA380182369 | ALX4 | c.667A>C (p.Ser223Arg) c.145A>C (p.Ser49Arg) | |
| 11 | g.44275459G>A | CA474035575 | ALX4 | c.666C>T (p.Thr222=) c.144C>T (p.Thr48=) | dbSNP gnomAD v4 |
| 11 | g.44275459G>C | CA474035576 | ALX4 | c.666C>G (p.Thr222=) c.144C>G (p.Thr48=) | |
| 11 | g.44275459G= | CA1967929025 | ALX4 | c.666C= (p.Thr222=) c.144C= (p.Thr48=) | |
| 11 | g.44275459G>T | CA474035577 | ALX4 | c.666C>A (p.Thr222=) c.144C>A (p.Thr48=) | |
| 11 | g.44275460G>A | CA380182372 | ALX4 | c.665C>T (p.Thr222Ile) c.143C>T (p.Thr48Ile) | |
| 11 | g.44275460G>C | CA380182373 | ALX4 | c.665C>G (p.Thr222Ser) c.143C>G (p.Thr48Ser) | gnomAD v4 |
| 11 | g.44275460G>T | CA380182374 | ALX4 | c.665C>A (p.Thr222Asn) c.143C>A (p.Thr48Asn) | |
| 11 | g.44275461T>A | CA380182375 | ALX4 | c.664A>T (p.Thr222Ser) c.142A>T (p.Thr48Ser) | |
| 11 | g.44275461T>C | CA380182376 | ALX4 | c.664A>G (p.Thr222Ala) c.142A>G (p.Thr48Ala) | COSMIC |
| 11 | g.44275461T>G | CA380182377 | ALX4 | c.664A>C (p.Thr222Pro) c.142A>C (p.Thr48Pro) | gnomAD v4 |
| 11 | g.44275462G>A | CA5955680 | ALX4 | c.663C>T (p.Phe221=) c.141C>T (p.Phe47=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 11 | g.44275462G>C | CA380182379 | ALX4 | c.663C>G (p.Phe221Leu) c.141C>G (p.Phe47Leu) | |
| 11 | g.44275462G= | CA1967929027 | ALX4 | c.663C= (p.Phe221=) c.141C= (p.Phe47=) | |
| 11 | g.44275462G>T | CA380182378 | ALX4 | c.663C>A (p.Phe221Leu) c.141C>A (p.Phe47Leu) | |
| 11 | g.44275463A>C | CA380182380 | ALX4 | c.662T>G (p.Phe221Cys) c.140T>G (p.Phe47Cys) | |
| 11 | g.44275463A>G | CA380182381 | ALX4 | c.662T>C (p.Phe221Ser) c.140T>C (p.Phe47Ser) | |
| 11 | g.44275463A>T | CA380182382 | ALX4 | c.662T>A (p.Phe221Tyr) c.140T>A (p.Phe47Tyr) | |
| 11 | g.44275464A>C | CA380182383 | ALX4 | c.661T>G (p.Phe221Val) c.139T>G (p.Phe47Val) | |
| 11 | g.44275464A>G | CA380182384 | ALX4 | c.661T>C (p.Phe221Leu) c.139T>C (p.Phe47Leu) | |
| 11 | g.44275464A>T | CA380182385 | ALX4 | c.661T>A (p.Phe221Ile) c.139T>A (p.Phe47Ile) | |
| 11 | g.44275465G>A | CA474035586 | ALX4 | c.660C>T (p.Thr220=) c.138C>T (p.Thr46=) | COSMIC |
| 11 | g.44275465G>C | CA474035588 | ALX4 | c.660C>G (p.Thr220=) c.138C>G (p.Thr46=) | |
| 11 | g.44275465G>T | CA474035585 | ALX4 | c.660C>A (p.Thr220=) c.138C>A (p.Thr46=) | |
| 11 | g.44275466G>A | CA380182386 | ALX4 | c.659C>T (p.Thr220Ile) c.137C>T (p.Thr46Ile) | |
| 11 | g.44275466G>C | CA380182388 | ALX4 | c.659C>G (p.Thr220Ser) c.137C>G (p.Thr46Ser) | |
| 11 | g.44275466G>T | CA380182387 | ALX4 | c.659C>A (p.Thr220Asn) c.137C>A (p.Thr46Asn) | |
| 11 | g.44275467T>A | CA380182389 | ALX4 | c.658A>T (p.Thr220Ser) c.136A>T (p.Thr46Ser) | gnomAD v4 |
| 11 | g.44275467T>C | CA380182390 | ALX4 | c.658A>G (p.Thr220Ala) c.136A>G (p.Thr46Ala) | |
| 11 | g.44275467T>G | CA380182391 | ALX4 | c.658A>C (p.Thr220Pro) c.136A>C (p.Thr46Pro) | dbSNP |
| 11 | g.44275467T= | CA1967929033 | ALX4 | c.658A= (p.Thr220=) c.136A= (p.Thr46=) | |
| 11 | g.44275468G>A | CA221497548 | ALX4 | c.657C>T (p.Thr219=) c.135C>T (p.Thr45=) | dbSNP |
| 11 | g.44275468G>C | CA474035595 | ALX4 | c.657C>G (p.Thr219=) c.135C>G (p.Thr45=) | |
| 11 | g.44275468G= | CA1967929036 | ALX4 | c.657C= (p.Thr219=) c.135C= (p.Thr45=) | |
| 11 | g.44275468G>T | CA474035599 | ALX4 | c.657C>A (p.Thr219=) c.135C>A (p.Thr45=) | dbSNP gnomAD v3 gnomAD v4 |
| 11 | g.44275469G>A | CA380182392 | ALX4 | c.656C>T (p.Thr219Ile) c.134C>T (p.Thr45Ile) | gnomAD v4 |
| 11 | g.44275469G>C | CA380182393 | ALX4 | c.656C>G (p.Thr219Ser) c.134C>G (p.Thr45Ser) | |
| 11 | g.44275469G>T | CA380182394 | ALX4 | c.656C>A (p.Thr219Asn) c.134C>A (p.Thr45Asn) | |
| 11 | g.44275470T>A | CA380182395 | ALX4 | c.655A>T (p.Thr219Ser) c.133A>T (p.Thr45Ser) | |
| 11 | g.44275470T>C | CA380182396 | ALX4 | c.655A>G (p.Thr219Ala) c.133A>G (p.Thr45Ala) | |
| 11 | g.44275470T>G | CA380182397 | ALX4 | c.655A>C (p.Thr219Pro) c.133A>C (p.Thr45Pro) | |
| 11 | g.44275471C>A | CA474035612 | ALX4 | c.654G>T (p.Arg218=) c.132G>T (p.Arg44=) | |
| 11 | g.44275471C>G | CA474035609 | ALX4 | c.654G>C (p.Arg218=) c.132G>C (p.Arg44=) | |
| 11 | g.44275471C>T | CA474035610 | ALX4 | c.654G>A (p.Arg218=) c.132G>A (p.Arg44=) | |
| 11 | g.44275472C>A | CA380182398 | ALX4 | c.653G>T (p.Arg218Leu) c.131G>T (p.Arg44Leu) | |
| 11 | g.44275472C= | CA1967929042 | ALX4 | c.653G= (p.Arg218=) c.131G= (p.Arg44=) | |
| 11 | g.44275472C>G | CA380182399 | ALX4 | c.653G>C (p.Arg218Pro) c.131G>C (p.Arg44Pro) | |
| 11 | g.44275472C>T | CA340336 | ALX4 | c.653G>A (p.Arg218Gln) c.131G>A (p.Arg44Gln) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
| 11 | g.44275473G>A | CA221497557 | ALX4 | c.652C>T (p.Arg218Trp) c.130C>T (p.Arg44Trp) | dbSNP gnomAD v2 gnomAD v4 COSMIC |
| 11 | g.44275473G>C | CA380182400 | ALX4 | c.652C>G (p.Arg218Gly) c.130C>G (p.Arg44Gly) | |
| 11 | g.44275473G= | CA1967929049 | ALX4 | c.652C= (p.Arg218=) c.130C= (p.Arg44=) | |
| 11 | g.44275473G>T | CA5955681 | ALX4 | c.652C>A (p.Arg218=) c.130C>A (p.Arg44=) | dbSNP ExAC gnomAD v3 gnomAD v4 |
| 11 | g.44275474G>A | CA474035622 | ALX4 | c.651C>T (p.Asn217=) c.129C>T (p.Asn43=) | |
| 11 | g.44275474G>C | CA380182401 | ALX4 | c.651C>G (p.Asn217Lys) c.129C>G (p.Asn43Lys) | dbSNP |
| 11 | g.44275474G= | CA1967929053 | ALX4 | c.651C= (p.Asn217=) c.129C= (p.Asn43=) | |
| 11 | g.44275474G>T | CA380182402 | ALX4 | c.651C>A (p.Asn217Lys) c.129C>A (p.Asn43Lys) | dbSNP |
| 11 | g.44275475T>A | CA380182403 | ALX4 | c.650A>T (p.Asn217Ile) c.128A>T (p.Asn43Ile) | |
| 11 | g.44275475T>C | CA380182404 | ALX4 | c.650A>G (p.Asn217Ser) c.128A>G (p.Asn43Ser) | |
| 11 | g.44275475T>G | CA380182405 | ALX4 | c.650A>C (p.Asn217Thr) c.128A>C (p.Asn43Thr) | |
| 11 | g.44275476T>A | CA380182406 | ALX4 | c.649A>T (p.Asn217Tyr) c.127A>T (p.Asn43Tyr) | |
| 11 | g.44275476T>C | CA380182407 | ALX4 | c.649A>G (p.Asn217Asp) c.127A>G (p.Asn43Asp) | |
| 11 | g.44275476T>G | CA380182408 | ALX4 | c.649A>C (p.Asn217His) c.127A>C (p.Asn43His) | |
| 11 | g.44275477C>A | CA474035630 | ALX4 | c.648G>T (p.Arg216=) c.126G>T (p.Arg42=) | |
| 11 | g.44275477C= | CA1967929056 | ALX4 | c.648G= (p.Arg216=) c.126G= (p.Arg42=) | |
| 11 | g.44275477C>G | CA474035629 | ALX4 | c.648G>C (p.Arg216=) c.126G>C (p.Arg42=) | |
| 11 | g.44275477C>T | CA5955682 | ALX4 | c.648G>A (p.Arg216=) c.126G>A (p.Arg42=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 11 | g.44275478C>A | CA380182409 | ALX4 | c.647G>T (p.Arg216Leu) c.125G>T (p.Arg42Leu) | |
| 11 | g.44275478C= | CA1967929060 | ALX4 | c.647G= (p.Arg216=) c.125G= (p.Arg42=) | |
| 11 | g.44275478C>G | CA380182410 | ALX4 | c.647G>C (p.Arg216Pro) c.125G>C (p.Arg42Pro) | |
| 11 | g.44275478C>T | CA221497573 | ALX4 | c.647G>A (p.Arg216Gln) c.125G>A (p.Arg42Gln) | dbSNP gnomAD v3 gnomAD v4 |
| 11 | g.44275479G>A | CA5955683 | ALX4 | c.646C>T (p.Arg216Trp) c.124C>T (p.Arg42Trp) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 11 | g.44275479G>C | CA270668 | ALX4 | c.646C>G (p.Arg216Gly) c.124C>G (p.Arg42Gly) | ClinVar dbSNP gnomAD v4 |
| 11 | g.44275479G= | CA1967929065 | ALX4 | c.646C= (p.Arg216=) c.124C= (p.Arg42=) | |
| 11 | g.44275479G>T | CA474035634 | ALX4 | c.646C>A (p.Arg216=) c.124C>A (p.Arg42=) | |
| 11 | g.44275480C>A | CA474035636 | ALX4 | c.645G>T (p.Arg215=) c.123G>T (p.Arg41=) | |
| 11 | g.44275480C>G | CA474035637 | ALX4 | c.645G>C (p.Arg215=) c.123G>C (p.Arg41=) | |
| 11 | g.44275480C>T | CA474035639 | ALX4 | c.645G>A (p.Arg215=) c.123G>A (p.Arg41=) | gnomAD v4 |
| 11 | g.44275481C>A | CA380182411 | ALX4 | c.644G>T (p.Arg215Leu) c.122G>T (p.Arg41Leu) | gnomAD v4 |
| 11 | g.44275481C= | CA1967929073 | ALX4 | c.644G= (p.Arg215=) c.122G= (p.Arg41=) | |
| 11 | g.44275481C>G | CA380182412 | ALX4 | c.644G>C (p.Arg215Pro) c.122G>C (p.Arg41Pro) | |
| 11 | g.44275481C>T | CA5955684 | ALX4 | c.644G>A (p.Arg215Gln) c.122G>A (p.Arg41Gln) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.44275482G>A | CA5955685 | ALX4 | c.643C>T (p.Arg215Trp) c.121C>T (p.Arg41Trp) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.44275482G>C | CA380182413 | ALX4 | c.643C>G (p.Arg215Gly) c.121C>G (p.Arg41Gly) | COSMIC |
| 11 | g.44275482G= | CA1967929079 | ALX4 | c.643C= (p.Arg215=) c.121C= (p.Arg41=) | |
| 11 | g.44275482G>T | CA474035643 | ALX4 | c.643C>A (p.Arg215=) c.121C>A (p.Arg41=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 11 | g.44275483C>A | CA380182414 | ALX4 | c.642G>T (p.Lys214Asn) c.120G>T (p.Lys40Asn) | |
| 11 | g.44275483C>G | CA380182415 | ALX4 | c.642G>C (p.Lys214Asn) c.120G>C (p.Lys40Asn) | |
| 11 | g.44275483C>T | CA474035647 | ALX4 | c.642G>A (p.Lys214=) c.120G>A (p.Lys40=) | |
| 11 | g.44275484T>A | CA380182416 | ALX4 | c.641A>T (p.Lys214Met) c.119A>T (p.Lys40Met) | |
| 11 | g.44275484T>C | CA380182417 | ALX4 | c.641A>G (p.Lys214Arg) c.119A>G (p.Lys40Arg) | |
| 11 | g.44275484T>G | CA380182418 | ALX4 | c.641A>C (p.Lys214Thr) c.119A>C (p.Lys40Thr) | |
| 11 | g.44275485T>A | CA380182419 | ALX4 | c.640A>T (p.Lys214Ter) c.118A>T (p.Lys40Ter) | |
| 11 | g.44275485T>C | CA380182420 | ALX4 | c.640A>G (p.Lys214Glu) c.118A>G (p.Lys40Glu) | |
| 11 | g.44275485T>G | CA380182421 | ALX4 | c.640A>C (p.Lys214Gln) c.118A>C (p.Lys40Gln) | |
| 11 | g.44275486C>A | CA380182422 | ALX4 | c.639G>T (p.Lys213Asn) c.117G>T (p.Lys39Asn) | gnomAD v4 |
| 11 | g.44275486C>G | CA380182423 | ALX4 | c.639G>C (p.Lys213Asn) c.117G>C (p.Lys39Asn) | |
| 11 | g.44275486C>T | CA474035652 | ALX4 | c.639G>A (p.Lys213=) c.117G>A (p.Lys39=) | |
| 11 | g.44275487T>A | CA380182424 | ALX4 | c.638A>T (p.Lys213Met) c.116A>T (p.Lys39Met) | |
| 11 | g.44275487T>C | CA380182426 | ALX4 | c.638A>G (p.Lys213Arg) c.116A>G (p.Lys39Arg) | COSMIC |
| 11 | g.44275487T>G | CA380182425 | ALX4 | c.638A>C (p.Lys213Thr) c.116A>C (p.Lys39Thr) | |
| 11 | g.44275488T>A | CA380182427 | ALX4 | c.637A>T (p.Lys213Ter) c.115A>T (p.Lys39Ter) | |
| 11 | g.44275488T>C | CA380182429 | ALX4 | c.637A>G (p.Lys213Glu) c.115A>G (p.Lys39Glu) | |
| 11 | g.44275488T>G | CA380182428 | ALX4 | c.637A>C (p.Lys213Gln) c.115A>C (p.Lys39Gln) | |
| 11 | g.44275489G>A | CA474035654 | ALX4 | c.636C>T (p.Gly212=) c.114C>T (p.Gly38=) | |
| 11 | g.44275489G>C | CA5955686 | ALX4 | c.636C>G (p.Gly212=) c.114C>G (p.Gly38=) | dbSNP ExAC gnomAD v2 |
| 11 | g.44275489G= | CA1967929087 | ALX4 | c.636C= (p.Gly212=) c.114C= (p.Gly38=) | |
| 11 | g.44275489G>T | CA474035656 | ALX4 | c.636C>A (p.Gly212=) c.114C>A (p.Gly38=) | dbSNP |
| 11 | g.44275490C>A | CA380182430 | ALX4 | c.635G>T (p.Gly212Val) c.113G>T (p.Gly38Val) | |
| 11 | g.44275490C>G | CA380182431 | ALX4 | c.635G>C (p.Gly212Ala) c.113G>C (p.Gly38Ala) | |
| 11 | g.44275490C>T | CA380182432 | ALX4 | c.635G>A (p.Gly212Asp) c.113G>A (p.Gly38Asp) | |
| 11 | g.44275491C>A | CA380182433 | ALX4 | c.634G>T (p.Gly212Cys) c.112G>T (p.Gly38Cys) | |
| 11 | g.44275491C>G | CA380182434 | ALX4 | c.634G>C (p.Gly212Arg) c.112G>C (p.Gly38Arg) | |
| 11 | g.44275491C>T | CA380182435 | ALX4 | c.634G>A (p.Gly212Ser) c.112G>A (p.Gly38Ser) | gnomAD v4 |
| 11 | g.44275492C>A | CA380182436 | ALX4 | c.633G>T (p.Lys211Asn) c.111G>T (p.Lys37Asn) | |
| 11 | g.44275492C= | CA1967929089 | ALX4 | c.633G= (p.Lys211=) c.111G= (p.Lys37=) | |
| 11 | g.44275492C>G | CA380182437 | ALX4 | c.633G>C (p.Lys211Asn) c.111G>C (p.Lys37Asn) | dbSNP |
| 11 | g.44275492C>T | CA474035660 | ALX4 | c.633G>A (p.Lys211=) c.111G>A (p.Lys37=) | gnomAD v4 |
| 11 | g.44275493T>A | CA380182438 | ALX4 | c.632A>T (p.Lys211Met) c.110A>T (p.Lys37Met) | |
| 11 | g.44275493T>C | CA380182439 | ALX4 | c.632A>G (p.Lys211Arg) c.110A>G (p.Lys37Arg) | |
| 11 | g.44275493T>G | CA380182440 | ALX4 | c.632A>C (p.Lys211Thr) c.110A>C (p.Lys37Thr) | dbSNP gnomAD v3 gnomAD v4 |
| 11 | g.44275493T= | CA1967929092 | ALX4 | c.632A= (p.Lys211=) c.110A= (p.Lys37=) | |
| 11 | g.44275494T>A | CA380182441 | ALX4 | c.631A>T (p.Lys211Ter) c.109A>T (p.Lys37Ter) | |
| 11 | g.44275494T>C | CA145363 | ALX4 | c.631A>G (p.Lys211Glu) c.109A>G (p.Lys37Glu) | ClinVar dbSNP gnomAD v4 |
| 11 | g.44275494T>G | CA380182442 | ALX4 | c.631A>C (p.Lys211Gln) c.109A>C (p.Lys37Gln) | |
| 11 | g.44275494T= | CA1967929096 | ALX4 | c.631A= (p.Lys211=) c.109A= (p.Lys37=) | |
| 11 | g.44275495G>A | CA5955687 | ALX4 | c.630C>T (p.Asn210=) c.108C>T (p.Asn36=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 11 | g.44275495G>C | CA380182443 | ALX4 | c.630C>G (p.Asn210Lys) c.108C>G (p.Asn36Lys) | |
| 11 | g.44275495G= | CA1967929101 | ALX4 | c.630C= (p.Asn210=) c.108C= (p.Asn36=) | |
| 11 | g.44275495G>T | CA380182444 | ALX4 | c.630C>A (p.Asn210Lys) c.108C>A (p.Asn36Lys) | |
| 11 | g.44275496T>A | CA380182445 | ALX4 | c.629A>T (p.Asn210Ile) c.107A>T (p.Asn36Ile) | |
| 11 | g.44275496T>C | CA380182446 | ALX4 | c.629A>G (p.Asn210Ser) c.107A>G (p.Asn36Ser) | gnomAD v4 |
| 11 | g.44275496T>G | CA380182447 | ALX4 | c.629A>C (p.Asn210Thr) c.107A>C (p.Asn36Thr) | |
| 11 | g.44275497T>A | CA380182448 | ALX4 | c.628A>T (p.Asn210Tyr) c.106A>T (p.Asn36Tyr) | |
| 11 | g.44275497T>C | CA380182449 | ALX4 | c.628A>G (p.Asn210Asp) c.106A>G (p.Asn36Asp) | |
| 11 | g.44275497T>G | CA380182450 | ALX4 | c.628A>C (p.Asn210His) c.106A>C (p.Asn36His) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.44275497T= | CA1967929104 | ALX4 | c.628A= (p.Asn210=) c.106A= (p.Asn36=) | |
| 11 | g.44275498G>A | CA474035665 | ALX4 | c.627C>T (p.Ser209=) c.105C>T (p.Ser35=) | gnomAD v4 |
| 11 | g.44275498G>C | CA380182451 | ALX4 | c.627C>G (p.Ser209Arg) c.105C>G (p.Ser35Arg) | |
| 11 | g.44275498G= | CA1967929108 | ALX4 | c.627C= (p.Ser209=) c.105C= (p.Ser35=) | |
| 11 | g.44275498G>T | CA5955688 | ALX4 | c.627C>A (p.Ser209Arg) c.105C>A (p.Ser35Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.44275499C>A | CA380182452 | ALX4 | c.626G>T (p.Ser209Ile) c.104G>T (p.Ser35Ile) | |
| 11 | g.44275499C= | CA1967929111 | ALX4 | c.626G= (p.Ser209=) c.104G= (p.Ser35=) | |
| 11 | g.44275499C>G | CA380182453 | ALX4 | c.626G>C (p.Ser209Thr) c.104G>C (p.Ser35Thr) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.44275499C>T | CA380182454 | ALX4 | c.626G>A (p.Ser209Asn) c.104G>A (p.Ser35Asn) | gnomAD v4 |
| 11 | g.44275500T>A | CA380182455 | ALX4 | c.625A>T (p.Ser209Cys) c.103A>T (p.Ser35Cys) | |
| 11 | g.44275500T>C | CA380182456 | ALX4 | c.625A>G (p.Ser209Gly) c.103A>G (p.Ser35Gly) | |
| 11 | g.44275500T>G | CA380182457 | ALX4 | c.625A>C (p.Ser209Arg) c.103A>C (p.Ser35Arg) |