Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
4 | g.67753825C>A | CA98671906 | GNRHR | c.511G>T (p.Ala171Ser) | dbSNP |
4 | g.67753825C= | CA1465420451 | GNRHR | c.511G= (p.Ala171=) | |
4 | g.67753825C>G | CA357054295 | GNRHR | c.511G>C (p.Ala171Pro) | |
4 | g.67753825C>T | CA130210 | GNRHR | c.511G>A (p.Ala171Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.67753826A= | CA1465420457 | GNRHR | c.510T= (p.Phe170=) | |
4 | g.67753826A>C | CA357054296 | GNRHR | c.510T>G (p.Phe170Leu) | |
4 | g.67753826A>G | CA439928838 | GNRHR | c.510T>C (p.Phe170=) | dbSNP gnomAD v4 |
4 | g.67753826A>T | CA357054297 | GNRHR | c.510T>A (p.Phe170Leu) | |
4 | g.67753827A>C | CA357054298 | GNRHR | c.509T>G (p.Phe170Cys) | |
4 | g.67753827A>G | CA357054299 | GNRHR | c.509T>C (p.Phe170Ser) | |
4 | g.67753827A>T | CA357054300 | GNRHR | c.509T>A (p.Phe170Tyr) | |
4 | g.67753828A>C | CA357054301 | GNRHR | c.508T>G (p.Phe170Val) | |
4 | g.67753828A>G | CA357054303 | GNRHR | c.508T>C (p.Phe170Leu) | |
4 | g.67753828A>T | CA357054302 | GNRHR | c.508T>A (p.Phe170Ile) | |
4 | g.67753829G>A | CA439928871 | GNRHR | c.507C>T (p.Val169=) | |
4 | g.67753829G>C | CA439928880 | GNRHR | c.507C>G (p.Val169=) | |
4 | g.67753829G>T | CA439928883 | GNRHR | c.507C>A (p.Val169=) | |
4 | g.67753830A= | CA1465420461 | GNRHR | c.506T= (p.Val169=) | |
4 | g.67753830A>C | CA357054304 | GNRHR | c.506T>G (p.Val169Gly) | dbSNP gnomAD v2 gnomAD v4 |
4 | g.67753830A>G | CA357054305 | GNRHR | c.506T>C (p.Val169Ala) | gnomAD v4 |
4 | g.67753830A>T | CA357054306 | GNRHR | c.506T>A (p.Val169Asp) | |
4 | g.67753831C>A | CA357054307 | GNRHR | c.505G>T (p.Val169Phe) | |
4 | g.67753831C>G | CA357054308 | GNRHR | c.505G>C (p.Val169Leu) | |
4 | g.67753831C>T | CA357054309 | GNRHR | c.505G>A (p.Val169Ile) | gnomAD v4 |
4 | g.67753832A= | CA1465420468 | GNRHR | c.504T= (p.Ser168=) | |
4 | g.67753832A>C | CA357054310 | GNRHR | c.504T>G (p.Ser168Arg) | |
4 | g.67753832A>G | CA439928918 | GNRHR | c.504T>C (p.Ser168=) | |
4 | g.67753832A>T | CA130205 | GNRHR | c.504T>A (p.Ser168Arg) | ClinVar dbSNP |
4 | g.67753833C>A | CA357054312 | GNRHR | c.503G>T (p.Ser168Ile) | |
4 | g.67753833C= | CA1465420472 | GNRHR | c.503G= (p.Ser168=) | |
4 | g.67753833C>G | CA357054313 | GNRHR | c.503G>C (p.Ser168Thr) | |
4 | g.67753833C>T | CA357054311 | GNRHR | c.503G>A (p.Ser168Asn) | dbSNP gnomAD v4 |
4 | g.67753834T>A | CA357054314 | GNRHR | c.502A>T (p.Ser168Cys) | |
4 | g.67753834T>C | CA357054315 | GNRHR | c.502A>G (p.Ser168Gly) | |
4 | g.67753834T>G | CA357054316 | GNRHR | c.502A>C (p.Ser168Arg) | |
4 | g.67753835A= | CA1465420477 | GNRHR | c.501T= (p.Ser167=) | |
4 | g.67753835A>C | CA98671910 | GNRHR | c.501T>G (p.Ser167Arg) | dbSNP |
4 | g.67753835A>G | CA439928941 | GNRHR | c.501T>C (p.Ser167=) | gnomAD v4 |
4 | g.67753835A>T | CA357054317 | GNRHR | c.501T>A (p.Ser167Arg) | dbSNP |
4 | g.67753836C>A | CA357054318 | GNRHR | c.500G>T (p.Ser167Ile) | |
4 | g.67753836C= | CA1465420479 | GNRHR | c.500G= (p.Ser167=) | |
4 | g.67753836C>G | CA357054319 | GNRHR | c.500G>C (p.Ser167Thr) | |
4 | g.67753836C>T | CA357054320 | GNRHR | c.500G>A (p.Ser167Asn) | dbSNP gnomAD v2 gnomAD v4 |
4 | g.67753837T>A | CA357054321 | GNRHR | c.499A>T (p.Ser167Cys) | |
4 | g.67753837T>C | CA357054322 | GNRHR | c.499A>G (p.Ser167Gly) | |
4 | g.67753837T>G | CA357054323 | GNRHR | c.499A>C (p.Ser167Arg) | |
4 | g.67753838G>A | CA439928968 | GNRHR | c.498C>T (p.Leu166=) | |
4 | g.67753838G>C | CA439928971 | GNRHR | c.498C>G (p.Leu166=) | dbSNP gnomAD v2 |
4 | g.67753838G= | CA1465420482 | GNRHR | c.498C= (p.Leu166=) | |
4 | g.67753838G>T | CA439928973 | GNRHR | c.498C>A (p.Leu166=) | COSMIC |