Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.225488869G>A | CA10753847 | ENAH | c.*8906C>T (n.*8906C>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.225488869G>C | CA2581705225 | ENAH | c.*8906C>G (n.*8906C>G) | |
1 | g.225488869G= | CA1140315274 | ENAH | c.*8906C= (n.*8906C=) | |
1 | g.225488869G>T | CA2581705224 | ENAH | c.*8906C>A (n.*8906C>A) | |
1 | g.225488871A>G | CA2747959140 | ENAH | c.*8904T>C (n.*8904T>C) | |
1 | g.225488873C= | CA1224492837 | ENAH | c.*8902G= (n.*8902G=) | |
1 | g.225488873C>T | CA529138973 | ENAH | c.*8902G>A (n.*8902G>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.225488874G>A | CA732233416 | ENAH | c.*8901C>T (n.*8901C>T) | dbSNP gnomAD v3 gnomAD v4 |
1 | g.225488874G= | CA1224492838 | ENAH | c.*8901C= (n.*8901C=) | |
1 | g.225488875G>A | CA2650717321 | ENAH | c.*8900C>T (n.*8900C>T) | gnomAD v4 |
1 | g.225488875G>T | CA2650717322 | ENAH | c.*8900C>A (n.*8900C>A) | gnomAD v4 |
1 | g.225488876C>A | CA2650717323 | ENAH | c.*8899G>T (n.*8899G>T) | gnomAD v4 |
1 | g.225488880T>A | CA2747959141 | ENAH | c.*8895A>T (n.*8895A>T) | |
1 | g.225488880T>C | CA10791718 | ENAH | c.*8895A>G (n.*8895A>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.225488880T>G | CA1224492839 | ENAH | c.*8895A>C (n.*8895A>C) | dbSNP |
1 | g.225488880T= | CA1140472340 | ENAH | c.*8895A= (n.*8895A=) | |
1 | g.225488881G>T | CA2650717324 | ENAH | c.*8894C>A (n.*8894C>A) | gnomAD v4 |
1 | g.225488882G>C | CA38523255 | ENAH | c.*8893C>G (n.*8893C>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.225488882G= | CA1224492840 | ENAH | c.*8893C= (n.*8893C=) | |
1 | g.225488884C>A | CA2650717325 | ENAH | c.*8891G>T (n.*8891G>T) | gnomAD v4 |
1 | g.225488885T>C | CA1012856336 | ENAH | c.*8890A>G (n.*8890A>G) | dbSNP gnomAD v3 gnomAD v4 |
1 | g.225488885T= | CA1224492841 | ENAH | c.*8890A= (n.*8890A=) | |
1 | g.225488886G>A | CA2650717326 | ENAH | c.*8889C>T (n.*8889C>T) | gnomAD v4 |
1 | g.225488887C>T | CA2650717327 | ENAH | c.*8888G>A (n.*8888G>A) | gnomAD v4 |
1 | g.225488888C= | CA1224492842 | ENAH | c.*8887G= (n.*8887G=) | |
1 | g.225488888C>T | CA38523258 | ENAH | c.*8887G>A (n.*8887G>A) | dbSNP gnomAD v3 gnomAD v4 |
1 | g.225488889A>G | CA2747959142 | ENAH | c.*8886T>C (n.*8886T>C) | |
1 | g.225488890A= | CA1224492844 | ENAH | c.*8885T= (n.*8885T=) | |
1 | g.225488890A>C | CA1224492843 | ENAH | c.*8885T>G (n.*8885T>G) | dbSNP |
1 | g.225488891G= | CA1224492845 | ENAH | c.*8884C= (n.*8884C=) | |
1 | g.225488891G>T | CA1224492846 | ENAH | c.*8884C>A (n.*8884C>A) | dbSNP gnomAD v4 |
1 | g.225488895T>C | CA1012856339 | ENAH | c.*8880A>G (n.*8880A>G) | dbSNP gnomAD v3 gnomAD v4 |
1 | g.225488895T= | CA1224492847 | ENAH | c.*8880A= (n.*8880A=) | |
1 | g.225488896T>C | CA2650717328 | ENAH | c.*8879A>G (n.*8879A>G) | gnomAD v4 |
1 | g.225488897G>A | CA1224492849 | ENAH | c.*8878C>T (n.*8878C>T) | dbSNP |
1 | g.225488897G= | CA1224492848 | ENAH | c.*8878C= (n.*8878C=) | |
1 | g.225488898C>A | CA2650717329 | ENAH | c.*8877G>T (n.*8877G>T) | gnomAD v4 |
1 | g.225488898C>T | CA2650717330 | ENAH | c.*8877G>A (n.*8877G>A) | gnomAD v4 |
1 | g.225488899T>C | CA2650717331 | ENAH | c.*8876A>G (n.*8876A>G) | gnomAD v4 |
1 | g.225488900G>A | CA1224492851 | ENAH | c.*8875C>T (n.*8875C>T) | dbSNP gnomAD v4 |
1 | g.225488900G= | CA1224492850 | ENAH | c.*8875C= (n.*8875C=) | |
1 | g.225488902T>G | CA38523264 | ENAH | c.*8873A>C (n.*8873A>C) | dbSNP gnomAD v3 gnomAD v4 |
1 | g.225488902T= | CA1224492853 | ENAH | c.*8873A= (n.*8873A=) | |
1 | g.225488902_225488903delinsTA | CA1224492852 | ENAH | c.*8872_*8873delinsTA (n.*8872_*8873delinsTA) | |
1 | g.225488902_225488903insTA | CA38523290 | ENAH | c.*8872_*8873insTA (n.*8872_*8873insTA) | dbSNP |
1 | g.225488903A= | CA1224492854 | ENAH | c.*8872T= (n.*8872T=) | |
1 | g.225488903A>G | CA38523288 | ENAH | c.*8872T>C (n.*8872T>C) | dbSNP |
1 | g.225488905del | CA38523275 | ENAH | c.*8872del (n.*8872del) | dbSNP |
1 | g.225488904A= | CA1224492855 | ENAH | c.*8871T= (n.*8871T=) | |
1 | g.225488904A>T | CA38523293 | ENAH | c.*8871T>A (n.*8871T>A) | dbSNP |