| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 9 | g.133256264G>A | CA040427 | ABO | c.467C>T (p.Pro156Leu) n.478C>T c.464C>T (p.Pro155Leu) | dbSNP ExAC gnomAD COSMIC |
| 9 | g.133256264G>C | CA375686297 | ABO | c.467C>G (p.Pro156Arg) n.478C>G c.464C>G (p.Pro155Arg) | |
| 9 | g.133256264G>T | CA375686298 | ABO | c.467C>A (p.Pro156Gln) n.478C>A c.464C>A (p.Pro155Gln) | |
| 9 | g.133256265G>A | CA375686301 | ABO | c.466C>T (p.Pro156Ser) n.477C>T c.463C>T (p.Pro155Ser) | |
| 9 | g.133256265G>C | CA375686299 | ABO | c.466C>G (p.Pro156Ala) n.477C>G c.463C>G (p.Pro155Ala) | |
| 9 | g.133256265G>T | CA375686300 | ABO | c.466C>A (p.Pro156Thr) n.477C>A c.463C>A (p.Pro155Thr) | |
| 9 | g.133256266C>A | CA375686302 | ABO | c.465G>T (p.Gln155His) n.476G>T c.462G>T (p.Gln154His) | |
| 9 | g.133256266C>G | CA375686303 | ABO | c.465G>C (p.Gln155His) n.476G>C c.462G>C (p.Gln154His) | |
| 9 | g.133256266C>T | CA200765562 | ABO | c.465G>A (p.Gln155=) n.476G>A c.462G>A (p.Gln154=) | dbSNP |
| 9 | g.133256267T>A | CA375686304 | ABO | c.464A>T (p.Gln155Leu) n.475A>T c.461A>T (p.Gln154Leu) | |
| 9 | g.133256267T>C | CA375686305 | ABO | c.464A>G (p.Gln155Arg) n.475A>G c.461A>G (p.Gln154Arg) | |
| 9 | g.133256267T>G | CA375686306 | ABO | c.464A>C (p.Gln155Pro) n.475A>C c.461A>C (p.Gln154Pro) | |
| 9 | g.133256268G>A | CA5305841 | ABO | c.463C>T (p.Gln155Ter) n.474C>T c.460C>T (p.Gln154Ter) | dbSNP ExAC gnomAD |
| 9 | g.133256268G>C | CA375686308 | ABO | c.463C>G (p.Gln155Glu) n.474C>G c.460C>G (p.Gln154Glu) | gnomAD |
| 9 | g.133256268G>T | CA375686307 | ABO | c.463C>A (p.Gln155Lys) n.474C>A c.460C>A (p.Gln154Lys) | |
| 9 | g.133256269G>A | CA5305842 | ABO | c.462C>T (p.Asp154=) n.473C>T c.459C>T (p.Asp153=) | dbSNP ExAC gnomAD |
| 9 | g.133256269G>C | CA375686309 | ABO | c.462C>G (p.Asp154Glu) n.473C>G c.459C>G (p.Asp153Glu) | |
| 9 | g.133256269G>T | CA375686310 | ABO | c.462C>A (p.Asp154Glu) n.473C>A c.459C>A (p.Asp153Glu) | |
| 9 | g.133256270T>A | CA375686311 | ABO | c.461A>T (p.Asp154Val) n.472A>T c.458A>T (p.Asp153Val) | |
| 9 | g.133256270T>C | CA375686312 | ABO | c.461A>G (p.Asp154Gly) n.472A>G c.458A>G (p.Asp153Gly) | |
| 9 | g.133256270T>G | CA375686313 | ABO | c.461A>C (p.Asp154Ala) n.472A>C c.458A>C (p.Asp153Ala) | |
| 9 | g.133256271C>A | CA375686314 | ABO | c.460G>T (p.Asp154Tyr) n.471G>T c.457G>T (p.Asp153Tyr) | |
| 9 | g.133256271C>G | CA375686315 | ABO | c.460G>C (p.Asp154His) n.471G>C c.457G>C (p.Asp153His) | |
| 9 | g.133256271C>T | CA200765570 | ABO | c.460G>A (p.Asp154Asn) n.471G>A c.457G>A (p.Asp153Asn) | dbSNP gnomAD COSMIC |
| 9 | g.133256272G>A | CA200765573 | ABO | c.459C>T (p.Thr153=) n.470C>T c.456C>T (p.Thr152=) | dbSNP |
| 9 | g.133256272G>C | CA467782935 | ABO | c.459C>G (p.Thr153=) n.470C>G c.456C>G (p.Thr152=) | |
| 9 | g.133256272G>T | CA467782937 | ABO | c.459C>A (p.Thr153=) n.470C>A c.456C>A (p.Thr152=) | |
| 9 | g.133256273G>A | CA375686316 | ABO | c.458C>T (p.Thr153Ile) n.469C>T c.455C>T (p.Thr152Ile) | |
| 9 | g.133256273G>C | CA375686317 | ABO | c.458C>G (p.Thr153Ser) n.469C>G c.455C>G (p.Thr152Ser) | gnomAD |
| 9 | g.133256273G>T | CA375686318 | ABO | c.458C>A (p.Thr153Asn) n.469C>A c.455C>A (p.Thr152Asn) | |
| 9 | g.133256274T>A | CA375686319 | ABO | c.457A>T (p.Thr153Ser) n.468A>T c.454A>T (p.Thr152Ser) | |
| 9 | g.133256274T>C | CA375686321 | ABO | c.457A>G (p.Thr153Ala) n.468A>G c.454A>G (p.Thr152Ala) | |
| 9 | g.133256274T>G | CA375686320 | ABO | c.457A>C (p.Thr153Pro) n.468A>C c.454A>C (p.Thr152Pro) | |
| 9 | g.133256275G>A | CA467782939 | ABO | c.456C>T (p.Phe152=) n.467C>T c.453C>T (p.Phe151=) | |
| 9 | g.133256275G>C | CA375686322 | ABO | c.456C>G (p.Phe152Leu) n.467C>G c.453C>G (p.Phe151Leu) | |
| 9 | g.133256275G>T | CA375686323 | ABO | c.456C>A (p.Phe152Leu) n.467C>A c.453C>A (p.Phe151Leu) | |
| 9 | g.133256276A>C | CA375686324 | ABO | c.455T>G (p.Phe152Cys) n.466T>G c.452T>G (p.Phe151Cys) | |
| 9 | g.133256276A>G | CA375686325 | ABO | c.455T>C (p.Phe152Ser) n.466T>C c.452T>C (p.Phe151Ser) | |
| 9 | g.133256276A>T | CA375686326 | ABO | c.455T>A (p.Phe152Tyr) n.466T>A c.452T>A (p.Phe151Tyr) | |
| 9 | g.133256277A>C | CA375686327 | ABO | c.454T>G (p.Phe152Val) n.465T>G c.451T>G (p.Phe151Val) | |
| 9 | g.133256277A>G | CA200765576 | ABO | c.454T>C (p.Phe152Leu) n.465T>C c.451T>C (p.Phe151Leu) | dbSNP gnomAD |
| 9 | g.133256277A>T | CA375686328 | ABO | c.454T>A (p.Phe152Ile) n.465T>A c.451T>A (p.Phe151Ile) | |
| 9 | g.133256278G>A | CA467782944 | ABO | c.453C>T (p.Val151=) n.464C>T c.450C>T (p.Val150=) | |
| 9 | g.133256278G>C | CA467782946 | ABO | c.453C>G (p.Val151=) n.464C>G c.450C>G (p.Val150=) | |
| 9 | g.133256278G>T | CA467782945 | ABO | c.453C>A (p.Val151=) n.464C>A c.450C>A (p.Val150=) | |
| 9 | g.133256279A>C | CA375686329 | ABO | c.452T>G (p.Val151Gly) n.463T>G c.449T>G (p.Val150Gly) | |
| 9 | g.133256279A>G | CA375686330 | ABO | c.452T>C (p.Val151Ala) n.463T>C c.449T>C (p.Val150Ala) | |
| 9 | g.133256279A>T | CA375686331 | ABO | c.452T>A (p.Val151Asp) n.463T>A c.449T>A (p.Val150Asp) | |
| 9 | g.133256280C>A | CA375686332 | ABO | c.451G>T (p.Val151Phe) n.462G>T c.448G>T (p.Val150Phe) | |
| 9 | g.133256280C>G | CA375686333 | ABO | c.451G>C (p.Val151Leu) n.462G>C c.448G>C (p.Val150Leu) |