Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
14 | g.105529621A>C | CA391203211 | TMEM121 | c.787A>C (p.Thr263Pro) | |
14 | g.105529621A>G | CA391203212 | TMEM121 | c.787A>G (p.Thr263Ala) | |
14 | g.105529621A>T | CA391203213 | TMEM121 | c.787A>T (p.Thr263Ser) | |
14 | g.105529622C>A | CA391203214 | TMEM121 | c.788C>A (p.Thr263Asn) | gnomAD v4 |
14 | g.105529622C= | CA2161352829 | TMEM121 | c.788C= (p.Thr263=) | |
14 | g.105529622C>G | CA391203215 | TMEM121 | c.788C>G (p.Thr263Ser) | dbSNP gnomAD v3 gnomAD v4 |
14 | g.105529622C>T | CA391203216 | TMEM121 | c.788C>T (p.Thr263Ile) | |
14 | g.105529623C>A | CA488509363 | TMEM121 | c.789C>A (p.Thr263=) | dbSNP gnomAD v2 gnomAD v4 |
14 | g.105529623C= | CA2161352830 | TMEM121 | c.789C= (p.Thr263=) | |
14 | g.105529623C>G | CA488509365 | TMEM121 | c.789C>G (p.Thr263=) | gnomAD v4 |
14 | g.105529623C>T | CA488509366 | TMEM121 | c.789C>T (p.Thr263=) | gnomAD v4 |
14 | g.105529624T>A | CA391203217 | TMEM121 | c.790T>A (p.Phe264Ile) | |
14 | g.105529624T>C | CA391203218 | TMEM121 | c.790T>C (p.Phe264Leu) | gnomAD v4 |
14 | g.105529624T>G | CA391203219 | TMEM121 | c.790T>G (p.Phe264Val) | |
14 | g.105529625T>A | CA391203221 | TMEM121 | c.791T>A (p.Phe264Tyr) | |
14 | g.105529625T>C | CA391203222 | TMEM121 | c.791T>C (p.Phe264Ser) | |
14 | g.105529625T>G | CA391203220 | TMEM121 | c.791T>G (p.Phe264Cys) | |
14 | g.105529626C>A | CA391203224 | TMEM121 | c.792C>A (p.Phe264Leu) | gnomAD v4 |
14 | g.105529626C= | CA2161352831 | TMEM121 | c.792C= (p.Phe264=) | |
14 | g.105529626C>G | CA391203223 | TMEM121 | c.792C>G (p.Phe264Leu) | |
14 | g.105529626C>T | CA488509372 | TMEM121 | c.792C>T (p.Phe264=) | dbSNP gnomAD v4 |
14 | g.105529627C>A | CA391203225 | TMEM121 | c.793C>A (p.Leu265Met) | gnomAD v4 |
14 | g.105529627C>G | CA391203226 | TMEM121 | c.793C>G (p.Leu265Val) | |
14 | g.105529627C>T | CA488509373 | TMEM121 | c.793C>T (p.Leu265=) | |
14 | g.105529628T>A | CA391203227 | TMEM121 | c.794T>A (p.Leu265Gln) | gnomAD v4 |
14 | g.105529628T>C | CA391203228 | TMEM121 | c.794T>C (p.Leu265Pro) | gnomAD v4 |
14 | g.105529628T>G | CA391203229 | TMEM121 | c.794T>G (p.Leu265Arg) | |
14 | g.105529629G>A | CA488509375 | TMEM121 | c.795G>A (p.Leu265=) | |
14 | g.105529629G>C | CA488509377 | TMEM121 | c.795G>C (p.Leu265=) | |
14 | g.105529629G>T | CA488509376 | TMEM121 | c.795G>T (p.Leu265=) | gnomAD v4 |
14 | g.105529630G>A | CA391203232 | TMEM121 | c.796G>A (p.Glu266Lys) | gnomAD v4 |
14 | g.105529630G>C | CA391203230 | TMEM121 | c.796G>C (p.Glu266Gln) | |
14 | g.105529630G>T | CA391203231 | TMEM121 | c.796G>T (p.Glu266Ter) | gnomAD v4 |
14 | g.105529631A>C | CA391203233 | TMEM121 | c.797A>C (p.Glu266Ala) | |
14 | g.105529631A>G | CA391203234 | TMEM121 | c.797A>G (p.Glu266Gly) | gnomAD v4 |
14 | g.105529631A>T | CA391203235 | TMEM121 | c.797A>T (p.Glu266Val) | |
14 | g.105529632_105529634del | CA2626945787 | TMEM121 | c.798_800del (p.Glu266_Tyr267delinsAsp) | gnomAD v4 |
14 | g.105529632G>A | CA488509384 | TMEM121 | c.798G>A (p.Glu266=) | dbSNP gnomAD v4 |
14 | g.105529632G>C | CA7391493 | TMEM121 | c.798G>C (p.Glu266Asp) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.105529632G= | CA2161352832 | TMEM121 | c.798G= (p.Glu266=) | |
14 | g.105529632G>T | CA391203236 | TMEM121 | c.798G>T (p.Glu266Asp) | gnomAD v4 |
14 | g.105529633T>A | CA391203237 | TMEM121 | c.799T>A (p.Tyr267Asn) | gnomAD v4 |
14 | g.105529633T>C | CA391203239 | TMEM121 | c.799T>C (p.Tyr267His) | gnomAD v4 |
14 | g.105529633T>G | CA391203238 | TMEM121 | c.799T>G (p.Tyr267Asp) | |
14 | g.105529634A>C | CA391203240 | TMEM121 | c.800A>C (p.Tyr267Ser) | |
14 | g.105529634A>G | CA391203241 | TMEM121 | c.800A>G (p.Tyr267Cys) | |
14 | g.105529634A>T | CA391203242 | TMEM121 | c.800A>T (p.Tyr267Phe) | |
14 | g.105529635C>A | CA391203243 | TMEM121 | c.801C>A (p.Tyr267Ter) | gnomAD v4 |
14 | g.105529635C>G | CA391203244 | TMEM121 | c.801C>G (p.Tyr267Ter) | |
14 | g.105529635C>T | CA488509388 | TMEM121 | c.801C>T (p.Tyr267=) | gnomAD v4 |