| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 20 | g.33438847_33438945del | CA2652478039 | SNTA1 | c.395_493del (p.Gly132_Leu164del) n.628_726del c.68_166del (p.Gly23_Leu55del) | gnomAD v4 |
| 20 | g.33438895G>A | CA408633407 | SNTA1 | c.442C>T (p.His148Tyr) n.675C>T c.115C>T (p.His39Tyr) | |
| 20 | g.33438895G>C | CA408633408 | SNTA1 | c.442C>G (p.His148Asp) n.675C>G c.115C>G (p.His39Asp) | |
| 20 | g.33438895G>T | CA408633409 | SNTA1 | c.442C>A (p.His148Asn) n.675C>A c.115C>A (p.His39Asn) | |
| 20 | g.33438896G>A | CA510252195 | SNTA1 | c.441C>T (p.Thr147=) n.674C>T c.114C>T (p.Thr38=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 20 | g.33438896G>C | CA510252197 | SNTA1 | c.441C>G (p.Thr147=) n.674C>G c.114C>G (p.Thr38=) | |
| 20 | g.33438896G= | CA2360753080 | SNTA1 | c.441C= (p.Thr147=) n.674C= c.114C= (p.Thr38=) | |
| 20 | g.33438896G>T | CA510252196 | SNTA1 | c.441C>A (p.Thr147=) n.674C>A c.114C>A (p.Thr38=) | |
| 20 | g.33438897G>A | CA9817226 | SNTA1 | c.440C>T (p.Thr147Ile) n.673C>T c.113C>T (p.Thr38Ile) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 20 | g.33438897G>C | CA408633410 | SNTA1 | c.440C>G (p.Thr147Ser) n.673C>G c.113C>G (p.Thr38Ser) | |
| 20 | g.33438897G= | CA2360753081 | SNTA1 | c.440C= (p.Thr147=) n.673C= c.113C= (p.Thr38=) | |
| 20 | g.33438897G>T | CA235722 | SNTA1 | c.440C>A (p.Thr147Asn) n.673C>A c.113C>A (p.Thr38Asn) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 20 | g.33438897_33438898delinsGT | CA2360753082 | SNTA1 | c.439_440delinsAC (p.Thr147=) n.672_673delinsAC c.112_113delinsAC (p.Thr38=) | |
| 20 | g.33438898del | CA743727207 | SNTA1 | c.439del (p.Thr147ProfsTer23) n.672del c.112del (p.Thr38ProfsTer23) | dbSNP |
| 20 | g.33438898T>A | CA408633413 | SNTA1 | c.439A>T (p.Thr147Ser) n.672A>T c.112A>T (p.Thr38Ser) | |
| 20 | g.33438898T>C | CA408633412 | SNTA1 | c.439A>G (p.Thr147Ala) n.672A>G c.112A>G (p.Thr38Ala) | |
| 20 | g.33438898T>G | CA408633411 | SNTA1 | c.439A>C (p.Thr147Pro) n.672A>C c.112A>C (p.Thr38Pro) | |
| 20 | g.33438899A>C | CA510252198 | SNTA1 | c.438T>G (p.Ala146=) n.671T>G c.111T>G (p.Ala37=) | |
| 20 | g.33438899A>G | CA510252200 | SNTA1 | c.438T>C (p.Ala146=) n.671T>C c.111T>C (p.Ala37=) | gnomAD v4 |
| 20 | g.33438899A>T | CA510252199 | SNTA1 | c.438T>A (p.Ala146=) n.671T>A c.111T>A (p.Ala37=) | |
| 20 | g.33438900G>A | CA408633414 | SNTA1 | c.437C>T (p.Ala146Val) n.670C>T c.110C>T (p.Ala37Val) | gnomAD v4 |
| 20 | g.33438900G>C | CA408633415 | SNTA1 | c.437C>G (p.Ala146Gly) n.670C>G c.110C>G (p.Ala37Gly) | |
| 20 | g.33438900G>T | CA408633416 | SNTA1 | c.437C>A (p.Ala146Asp) n.670C>A c.110C>A (p.Ala37Asp) | |
| 20 | g.33438901C>A | CA408633417 | SNTA1 | c.436G>T (p.Ala146Ser) n.669G>T c.109G>T (p.Ala37Ser) | |
| 20 | g.33438901C>G | CA408633418 | SNTA1 | c.436G>C (p.Ala146Pro) n.669G>C c.109G>C (p.Ala37Pro) | |
| 20 | g.33438901C>T | CA408633419 | SNTA1 | c.436G>A (p.Ala146Thr) n.669G>A c.109G>A (p.Ala37Thr) | |
| 20 | g.33438902A>C | CA510252203 | SNTA1 | c.435T>G (p.Ser145=) n.668T>G c.108T>G (p.Ser36=) | |
| 20 | g.33438902A>G | CA510252202 | SNTA1 | c.435T>C (p.Ser145=) n.668T>C c.108T>C (p.Ser36=) | |
| 20 | g.33438902A>T | CA510252201 | SNTA1 | c.435T>A (p.Ser145=) n.668T>A c.108T>A (p.Ser36=) | |
| 20 | g.33438903G>A | CA408633420 | SNTA1 | c.434C>T (p.Ser145Phe) n.667C>T c.107C>T (p.Ser36Phe) | |
| 20 | g.33438903G>C | CA408633421 | SNTA1 | c.434C>G (p.Ser145Cys) n.667C>G c.107C>G (p.Ser36Cys) | |
| 20 | g.33438903G>T | CA408633422 | SNTA1 | c.434C>A (p.Ser145Tyr) n.667C>A c.107C>A (p.Ser36Tyr) | |
| 20 | g.33438904A>C | CA408633423 | SNTA1 | c.433T>G (p.Ser145Ala) n.666T>G c.106T>G (p.Ser36Ala) | |
| 20 | g.33438904A>G | CA408633424 | SNTA1 | c.433T>C (p.Ser145Pro) n.666T>C c.106T>C (p.Ser36Pro) | |
| 20 | g.33438904A>T | CA408633425 | SNTA1 | c.433T>A (p.Ser145Thr) n.666T>A c.106T>A (p.Ser36Thr) | |
| 20 | g.33438905G>A | CA9817227 | SNTA1 | c.432C>T (p.Ser144=) n.665C>T c.105C>T (p.Ser35=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 20 | g.33438905G>C | CA510252205 | SNTA1 | c.432C>G (p.Ser144=) n.665C>G c.105C>G (p.Ser35=) | |
| 20 | g.33438905G= | CA2360753083 | SNTA1 | c.432C= (p.Ser144=) n.665C= c.105C= (p.Ser35=) | |
| 20 | g.33438905G>T | CA510252204 | SNTA1 | c.432C>A (p.Ser144=) n.665C>A c.105C>A (p.Ser35=) | |
| 20 | g.33438906G>A | CA9817228 | SNTA1 | c.431C>T (p.Ser144Phe) n.664C>T c.104C>T (p.Ser35Phe) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 20 | g.33438906G>C | CA408633426 | SNTA1 | c.431C>G (p.Ser144Cys) n.664C>G c.104C>G (p.Ser35Cys) | |
| 20 | g.33438906G= | CA2360753084 | SNTA1 | c.431C= (p.Ser144=) n.664C= c.104C= (p.Ser35=) | |
| 20 | g.33438906G>T | CA408633427 | SNTA1 | c.431C>A (p.Ser144Tyr) n.664C>A c.104C>A (p.Ser35Tyr) | |
| 20 | g.33438907A= | CA2360753085 | SNTA1 | c.430T= (p.Ser144=) n.663T= c.103T= (p.Ser35=) | |
| 20 | g.33438907A>C | CA9817229 | SNTA1 | c.430T>G (p.Ser144Ala) n.663T>G c.103T>G (p.Ser35Ala) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 20 | g.33438907A>G | CA408633428 | SNTA1 | c.430T>C (p.Ser144Pro) n.663T>C c.103T>C (p.Ser35Pro) | |
| 20 | g.33438907A>T | CA408633429 | SNTA1 | c.430T>A (p.Ser144Thr) n.663T>A c.103T>A (p.Ser35Thr) | |
| 20 | g.33438908C>A | CA408633430 | SNTA1 | c.429G>T (p.Leu143Phe) n.662G>T c.102G>T (p.Leu34Phe) | |
| 20 | g.33438908C>G | CA408633431 | SNTA1 | c.429G>C (p.Leu143Phe) n.662G>C c.102G>C (p.Leu34Phe) | |
| 20 | g.33438908C>T | CA510252206 | SNTA1 | c.429G>A (p.Leu143=) n.662G>A c.102G>A (p.Leu34=) | |
| 20 | g.33438909A>C | CA408633432 | SNTA1 | c.428T>G (p.Leu143Trp) n.661T>G c.101T>G (p.Leu34Trp) | |
| 20 | g.33438909A>G | CA408633434 | SNTA1 | c.428T>C (p.Leu143Ser) n.661T>C c.101T>C (p.Leu34Ser) | |
| 20 | g.33438909A>T | CA408633433 | SNTA1 | c.428T>A (p.Leu143Ter) n.661T>A c.101T>A (p.Leu34Ter) | |
| 20 | g.33438910A>C | CA408633435 | SNTA1 | c.427T>G (p.Leu143Val) n.660T>G c.100T>G (p.Leu34Val) | |
| 20 | g.33438910A>G | CA510252207 | SNTA1 | c.427T>C (p.Leu143=) n.660T>C c.100T>C (p.Leu34=) | |
| 20 | g.33438910A>T | CA408633436 | SNTA1 | c.427T>A (p.Leu143Met) n.660T>A c.100T>A (p.Leu34Met) | |
| 20 | g.33438911G>A | CA510252208 | SNTA1 | c.426C>T (p.Asp142=) n.659C>T c.99C>T (p.Asp33=) | |
| 20 | g.33438911G>C | CA408633437 | SNTA1 | c.426C>G (p.Asp142Glu) n.659C>G c.99C>G (p.Asp33Glu) | |
| 20 | g.33438911G>T | CA408633438 | SNTA1 | c.426C>A (p.Asp142Glu) n.659C>A c.99C>A (p.Asp33Glu) | |
| 20 | g.33438912T>A | CA408633439 | SNTA1 | c.425A>T (p.Asp142Val) n.658A>T c.98A>T (p.Asp33Val) | |
| 20 | g.33438912T>C | CA9817230 | SNTA1 | c.425A>G (p.Asp142Gly) n.658A>G c.98A>G (p.Asp33Gly) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 20 | g.33438912T>G | CA408633440 | SNTA1 | c.425A>C (p.Asp142Ala) n.658A>C c.98A>C (p.Asp33Ala) | |
| 20 | g.33438912T= | CA2360753086 | SNTA1 | c.425A= (p.Asp142=) n.658A= c.98A= (p.Asp33=) | |
| 20 | g.33438913C>A | CA408633441 | SNTA1 | c.424G>T (p.Asp142Tyr) n.657G>T c.97G>T (p.Asp33Tyr) | |
| 20 | g.33438913C= | CA2360753087 | SNTA1 | c.424G= (p.Asp142=) n.657G= c.97G= (p.Asp33=) | |
| 20 | g.33438913C>G | CA408633442 | SNTA1 | c.424G>C (p.Asp142His) n.657G>C c.97G>C (p.Asp33His) | |
| 20 | g.33438913C>T | CA408633443 | SNTA1 | c.424G>A (p.Asp142Asn) n.657G>A c.97G>A (p.Asp33Asn) | dbSNP |
| 20 | g.33438914T>A | CA408633444 | SNTA1 | c.423A>T (p.Glu141Asp) n.656A>T c.96A>T (p.Glu32Asp) | |
| 20 | g.33438914T>C | CA510252210 | SNTA1 | c.423A>G (p.Glu141=) n.656A>G c.96A>G (p.Glu32=) | |
| 20 | g.33438914T>G | CA408633445 | SNTA1 | c.423A>C (p.Glu141Asp) n.656A>C c.96A>C (p.Glu32Asp) | |
| 20 | g.33438915T>A | CA408633446 | SNTA1 | c.422A>T (p.Glu141Val) n.655A>T c.95A>T (p.Glu32Val) | |
| 20 | g.33438915T>C | CA408633447 | SNTA1 | c.422A>G (p.Glu141Gly) n.655A>G c.95A>G (p.Glu32Gly) | dbSNP |
| 20 | g.33438915T>G | CA408633448 | SNTA1 | c.422A>C (p.Glu141Ala) n.655A>C c.95A>C (p.Glu32Ala) | |
| 20 | g.33438915T= | CA2360753088 | SNTA1 | c.422A= (p.Glu141=) n.655A= c.95A= (p.Glu32=) | |
| 20 | g.33438916C>A | CA408633449 | SNTA1 | c.421G>T (p.Glu141Ter) n.654G>T c.94G>T (p.Glu32Ter) | |
| 20 | g.33438916C>G | CA408633450 | SNTA1 | c.421G>C (p.Glu141Gln) n.654G>C c.94G>C (p.Glu32Gln) | |
| 20 | g.33438916C>T | CA408633451 | SNTA1 | c.421G>A (p.Glu141Lys) n.654G>A c.94G>A (p.Glu32Lys) | |
| 20 | g.33438917C>A | CA510252211 | SNTA1 | c.420G>T (p.Gly140=) n.653G>T c.93G>T (p.Gly31=) | |
| 20 | g.33438917C>G | CA510252212 | SNTA1 | c.420G>C (p.Gly140=) n.653G>C c.93G>C (p.Gly31=) | COSMIC |
| 20 | g.33438917C>T | CA510252213 | SNTA1 | c.420G>A (p.Gly140=) n.653G>A c.93G>A (p.Gly31=) | |
| 20 | g.33438918C>A | CA408633452 | SNTA1 | c.419G>T (p.Gly140Val) n.652G>T c.92G>T (p.Gly31Val) | |
| 20 | g.33438918C= | CA2360753089 | SNTA1 | c.419G= (p.Gly140=) n.652G= c.92G= (p.Gly31=) | |
| 20 | g.33438918C>G | CA9817231 | SNTA1 | c.419G>C (p.Gly140Ala) n.652G>C c.92G>C (p.Gly31Ala) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 20 | g.33438918C>T | CA9817232 | SNTA1 | c.419G>A (p.Gly140Glu) n.652G>A c.92G>A (p.Gly31Glu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 20 | g.33438919C>A | CA408633455 | SNTA1 | c.418G>T (p.Gly140Trp) n.651G>T c.91G>T (p.Gly31Trp) | |
| 20 | g.33438919C= | CA2360753090 | SNTA1 | c.418G= (p.Gly140=) n.651G= c.91G= (p.Gly31=) | |
| 20 | g.33438919C>G | CA408633453 | SNTA1 | c.418G>C (p.Gly140Arg) n.651G>C c.91G>C (p.Gly31Arg) | |
| 20 | g.33438919C>T | CA408633454 | SNTA1 | c.418G>A (p.Gly140Arg) n.651G>A c.91G>A (p.Gly31Arg) | dbSNP |
| 20 | g.33438920A>C | CA408633456 | SNTA1 | c.417T>G (p.Asn139Lys) n.650T>G c.90T>G (p.Asn30Lys) | |
| 20 | g.33438920A>G | CA510252214 | SNTA1 | c.417T>C (p.Asn139=) n.650T>C c.90T>C (p.Asn30=) | |
| 20 | g.33438920A>T | CA408633457 | SNTA1 | c.417T>A (p.Asn139Lys) n.650T>A c.90T>A (p.Asn30Lys) | |
| 20 | g.33438921T>A | CA408633458 | SNTA1 | c.416A>T (p.Asn139Ile) n.649A>T c.89A>T (p.Asn30Ile) | |
| 20 | g.33438921T>C | CA408633459 | SNTA1 | c.416A>G (p.Asn139Ser) n.649A>G c.89A>G (p.Asn30Ser) | gnomAD v4 |
| 20 | g.33438921T>G | CA408633460 | SNTA1 | c.416A>C (p.Asn139Thr) n.649A>C c.89A>C (p.Asn30Thr) | |
| 20 | g.33438922T>A | CA408633461 | SNTA1 | c.415A>T (p.Asn139Tyr) n.648A>T c.88A>T (p.Asn30Tyr) | |
| 20 | g.33438922T>C | CA408633462 | SNTA1 | c.415A>G (p.Asn139Asp) n.648A>G c.88A>G (p.Asn30Asp) | |
| 20 | g.33438922T>G | CA408633463 | SNTA1 | c.415A>C (p.Asn139His) n.648A>C c.88A>C (p.Asn30His) | |
| 20 | g.33438923C>A | CA510252215 | SNTA1 | c.414G>T (p.Val138=) n.647G>T c.87G>T (p.Val29=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 20 | g.33438923C= | CA2360753091 | SNTA1 | c.414G= (p.Val138=) n.647G= c.87G= (p.Val29=) | |
| 20 | g.33438923C>G | CA510252216 | SNTA1 | c.414G>C (p.Val138=) n.647G>C c.87G>C (p.Val29=) | |
| 20 | g.33438923C>T | CA510252217 | SNTA1 | c.414G>A (p.Val138=) n.647G>A c.87G>A (p.Val29=) | |
| 20 | g.33438924A>C | CA408633464 | SNTA1 | c.413T>G (p.Val138Gly) n.646T>G c.86T>G (p.Val29Gly) | |
| 20 | g.33438924A>G | CA408633465 | SNTA1 | c.413T>C (p.Val138Ala) n.646T>C c.86T>C (p.Val29Ala) | |
| 20 | g.33438924A>T | CA408633466 | SNTA1 | c.413T>A (p.Val138Glu) n.646T>A c.86T>A (p.Val29Glu) | |
| 20 | g.33438925C>A | CA408633469 | SNTA1 | c.412G>T (p.Val138Leu) n.645G>T c.85G>T (p.Val29Leu) | |
| 20 | g.33438925C>G | CA408633467 | SNTA1 | c.412G>C (p.Val138Leu) n.645G>C c.85G>C (p.Val29Leu) | |
| 20 | g.33438925C>T | CA408633468 | SNTA1 | c.412G>A (p.Val138Met) n.645G>A c.85G>A (p.Val29Met) | |
| 20 | g.33438926A>C | CA510252218 | SNTA1 | c.411T>G (p.Ser137=) n.644T>G c.84T>G (p.Ser28=) | |
| 20 | g.33438926A>G | CA510252220 | SNTA1 | c.411T>C (p.Ser137=) n.644T>C c.84T>C (p.Ser28=) | |
| 20 | g.33438926A>T | CA510252219 | SNTA1 | c.411T>A (p.Ser137=) n.644T>A c.84T>A (p.Ser28=) | |
| 20 | g.33438927G>A | CA408633470 | SNTA1 | c.410C>T (p.Ser137Phe) n.643C>T c.83C>T (p.Ser28Phe) | |
| 20 | g.33438927G>C | CA408633471 | SNTA1 | c.410C>G (p.Ser137Cys) n.643C>G c.83C>G (p.Ser28Cys) | |
| 20 | g.33438927G>T | CA408633472 | SNTA1 | c.410C>A (p.Ser137Tyr) n.643C>A c.83C>A (p.Ser28Tyr) | |
| 20 | g.33438927_33438928insGT | CA2652478040 | SNTA1 | c.409_410insAC (p.Ser137TyrfsTer3) n.642_643insAC c.82_83insAC (p.Ser28TyrfsTer3) | gnomAD v4 |
| 20 | g.33438928A>C | CA408633473 | SNTA1 | c.409T>G (p.Ser137Ala) n.642T>G c.82T>G (p.Ser28Ala) | |
| 20 | g.33438928A>G | CA408633474 | SNTA1 | c.409T>C (p.Ser137Pro) n.642T>C c.82T>C (p.Ser28Pro) | |
| 20 | g.33438928A>T | CA408633475 | SNTA1 | c.409T>A (p.Ser137Thr) n.642T>A c.82T>A (p.Ser28Thr) | |
| 20 | g.33438929C>A | CA510252221 | SNTA1 | c.408G>T (p.Leu136=) n.641G>T c.81G>T (p.Leu27=) | |
| 20 | g.33438929C>G | CA510252222 | SNTA1 | c.408G>C (p.Leu136=) n.641G>C c.81G>C (p.Leu27=) | gnomAD v4 |
| 20 | g.33438929C>T | CA510252223 | SNTA1 | c.408G>A (p.Leu136=) n.641G>A c.81G>A (p.Leu27=) | gnomAD v4 |
| 20 | g.33438930A>C | CA408633476 | SNTA1 | c.407T>G (p.Leu136Arg) n.640T>G c.80T>G (p.Leu27Arg) | |
| 20 | g.33438930A>G | CA408633477 | SNTA1 | c.407T>C (p.Leu136Pro) n.640T>C c.80T>C (p.Leu27Pro) | |
| 20 | g.33438930A>T | CA408633478 | SNTA1 | c.407T>A (p.Leu136Gln) n.640T>A c.80T>A (p.Leu27Gln) | |
| 20 | g.33438931G>A | CA510252224 | SNTA1 | c.406C>T (p.Leu136=) n.639C>T c.79C>T (p.Leu27=) | |
| 20 | g.33438931G>C | CA408633479 | SNTA1 | c.406C>G (p.Leu136Val) n.639C>G c.79C>G (p.Leu27Val) | |
| 20 | g.33438931G>T | CA408633480 | SNTA1 | c.406C>A (p.Leu136Met) n.639C>A c.79C>A (p.Leu27Met) | |
| 20 | g.33438932G>A | CA510252225 | SNTA1 | c.405C>T (p.Ile135=) n.638C>T c.78C>T (p.Ile26=) | gnomAD v4 |
| 20 | g.33438932G>C | CA408633481 | SNTA1 | c.405C>G (p.Ile135Met) n.638C>G c.78C>G (p.Ile26Met) | |
| 20 | g.33438932G>T | CA510252226 | SNTA1 | c.405C>A (p.Ile135=) n.638C>A c.78C>A (p.Ile26=) | gnomAD v4 |
| 20 | g.33438933A>C | CA408633484 | SNTA1 | c.404T>G (p.Ile135Ser) n.637T>G c.77T>G (p.Ile26Ser) | |
| 20 | g.33438933A>G | CA408633483 | SNTA1 | c.404T>C (p.Ile135Thr) n.637T>C c.77T>C (p.Ile26Thr) | |
| 20 | g.33438933A>T | CA408633482 | SNTA1 | c.404T>A (p.Ile135Asn) n.637T>A c.77T>A (p.Ile26Asn) | |
| 20 | g.33438934T>A | CA408633486 | SNTA1 | c.403A>T (p.Ile135Phe) n.636A>T c.76A>T (p.Ile26Phe) | |
| 20 | g.33438934T>C | CA408633485 | SNTA1 | c.403A>G (p.Ile135Val) n.636A>G c.76A>G (p.Ile26Val) | |
| 20 | g.33438934T>G | CA302339 | SNTA1 | c.403A>C (p.Ile135Leu) n.636A>C c.76A>C (p.Ile26Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 20 | g.33438934T= | CA2360753092 | SNTA1 | c.403A= (p.Ile135=) n.636A= c.76A= (p.Ile26=) | |
| 20 | g.33438935G>A | CA510252229 | SNTA1 | c.402C>T (p.Ala134=) n.635C>T c.75C>T (p.Ala25=) | gnomAD v4 |
| 20 | g.33438935G>C | CA510252227 | SNTA1 | c.402C>G (p.Ala134=) n.635C>G c.75C>G (p.Ala25=) | |
| 20 | g.33438935G>T | CA510252228 | SNTA1 | c.402C>A (p.Ala134=) n.635C>A c.75C>A (p.Ala25=) | |
| 20 | g.33438936G>A | CA408633487 | SNTA1 | c.401C>T (p.Ala134Val) n.634C>T c.74C>T (p.Ala25Val) | |
| 20 | g.33438936G>C | CA408633488 | SNTA1 | c.401C>G (p.Ala134Gly) n.634C>G c.74C>G (p.Ala25Gly) | |
| 20 | g.33438936G>T | CA408633489 | SNTA1 | c.401C>A (p.Ala134Asp) n.634C>A c.74C>A (p.Ala25Asp) | |
| 20 | g.33438936_33438937insAAG | CA2652478041 | SNTA1 | c.401_402insTTC (p.Ala134_Ile135insSer) n.634_635insTTC c.74_75insTTC (p.Ala25_Ile26insSer) | gnomAD v4 |
| 20 | g.33438937C>A | CA408633490 | SNTA1 | c.400G>T (p.Ala134Ser) n.633G>T c.73G>T (p.Ala25Ser) | gnomAD v4 |
| 20 | g.33438937C>G | CA408633491 | SNTA1 | c.400G>C (p.Ala134Pro) n.633G>C c.73G>C (p.Ala25Pro) | |
| 20 | g.33438937C>T | CA408633492 | SNTA1 | c.400G>A (p.Ala134Thr) n.633G>A c.73G>A (p.Ala25Thr) | |
| 20 | g.33438938A= | CA2360753093 | SNTA1 | c.399T= (p.Asp133=) n.632T= c.72T= (p.Asp24=) | |
| 20 | g.33438938A>C | CA408633493 | SNTA1 | c.399T>G (p.Asp133Glu) n.632T>G c.72T>G (p.Asp24Glu) | |
| 20 | g.33438938A>G | CA313275662 | SNTA1 | c.399T>C (p.Asp133=) n.632T>C c.72T>C (p.Asp24=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 20 | g.33438938A>T | CA408633494 | SNTA1 | c.399T>A (p.Asp133Glu) n.632T>A c.72T>A (p.Asp24Glu) | |
| 20 | g.33438939T>A | CA408633495 | SNTA1 | c.398A>T (p.Asp133Val) n.631A>T c.71A>T (p.Asp24Val) | |
| 20 | g.33438939T>C | CA408633496 | SNTA1 | c.398A>G (p.Asp133Gly) n.631A>G c.71A>G (p.Asp24Gly) | dbSNP |
| 20 | g.33438939T>G | CA408633497 | SNTA1 | c.398A>C (p.Asp133Ala) n.631A>C c.71A>C (p.Asp24Ala) | |
| 20 | g.33438939T= | CA2360753094 | SNTA1 | c.398A= (p.Asp133=) n.631A= c.71A= (p.Asp24=) | |
| 20 | g.33438940C>A | CA408633499 | SNTA1 | c.397G>T (p.Asp133Tyr) n.630G>T c.70G>T (p.Asp24Tyr) | |
| 20 | g.33438940C>G | CA408633500 | SNTA1 | c.397G>C (p.Asp133His) n.630G>C c.70G>C (p.Asp24His) | |
| 20 | g.33438940C>T | CA408633498 | SNTA1 | c.397G>A (p.Asp133Asn) n.630G>A c.70G>A (p.Asp24Asn) | gnomAD v4 |
| 20 | g.33438941C>A | CA510252231 | SNTA1 | c.396G>T (p.Gly132=) n.629G>T c.69G>T (p.Gly23=) | |
| 20 | g.33438941C>G | CA510252230 | SNTA1 | c.396G>C (p.Gly132=) n.629G>C c.69G>C (p.Gly23=) | |
| 20 | g.33438941C>T | CA510252232 | SNTA1 | c.396G>A (p.Gly132=) n.629G>A c.69G>A (p.Gly23=) | |
| 20 | g.33438942C>A | CA408633501 | SNTA1 | c.395G>T (p.Gly132Val) n.628G>T c.68G>T (p.Gly23Val) | |
| 20 | g.33438942C>G | CA408633502 | SNTA1 | c.395G>C (p.Gly132Ala) n.628G>C c.68G>C (p.Gly23Ala) | |
| 20 | g.33438942C>T | CA408633503 | SNTA1 | c.395G>A (p.Gly132Glu) n.628G>A c.68G>A (p.Gly23Glu) | gnomAD v4 |
| 20 | g.33438943C>A | CA408633504 | SNTA1 | c.394G>T (p.Gly132Trp) n.627G>T c.67G>T (p.Gly23Trp) | |
| 20 | g.33438943C>G | CA408633505 | SNTA1 | c.394G>C (p.Gly132Arg) n.627G>C c.67G>C (p.Gly23Arg) | |
| 20 | g.33438943C>T | CA408633506 | SNTA1 | c.394G>A (p.Gly132Arg) n.627G>A c.67G>A (p.Gly23Arg) | |
| 20 | g.33438944C>A | CA510252233 | SNTA1 | c.393G>T (p.Val131=) n.626G>T c.66G>T (p.Val22=) | |
| 20 | g.33438944C>G | CA510252234 | SNTA1 | c.393G>C (p.Val131=) n.626G>C c.66G>C (p.Val22=) | |
| 20 | g.33438944C>T | CA510252235 | SNTA1 | c.393G>A (p.Val131=) n.626G>A c.66G>A (p.Val22=) | |
| 20 | g.33438945A>C | CA408633507 | SNTA1 | c.392T>G (p.Val131Gly) n.625T>G c.65T>G (p.Val22Gly) | |
| 20 | g.33438945A>G | CA408633509 | SNTA1 | c.392T>C (p.Val131Ala) n.625T>C c.65T>C (p.Val22Ala) | |
| 20 | g.33438945A>T | CA408633508 | SNTA1 | c.392T>A (p.Val131Glu) n.625T>A c.65T>A (p.Val22Glu) | |
| 20 | g.33438946C>A | CA408633510 | SNTA1 | c.391G>T (p.Val131Leu) n.624G>T c.64G>T (p.Val22Leu) | gnomAD v4 |
| 20 | g.33438946C>G | CA408633511 | SNTA1 | c.391G>C (p.Val131Leu) n.624G>C c.64G>C (p.Val22Leu) | |
| 20 | g.33438946C>T | CA408633512 | SNTA1 | c.391G>A (p.Val131Met) n.624G>A c.64G>A (p.Val22Met) | gnomAD v4 |
| 20 | g.33438947A>C | CA408633513 | SNTA1 | c.390T>G (p.Phe130Leu) n.623T>G c.63T>G (p.Phe21Leu) | |
| 20 | g.33438947A>G | CA510252238 | SNTA1 | c.390T>C (p.Phe130=) n.623T>C c.63T>C (p.Phe21=) | ClinVar dbSNP gnomAD v4 |
| 20 | g.33438947A>T | CA408633514 | SNTA1 | c.390T>A (p.Phe130Leu) n.623T>A c.63T>A (p.Phe21Leu) | |
| 20 | g.33438948A= | CA2360753095 | SNTA1 | c.389T= (p.Phe130=) n.622T= c.62T= (p.Phe21=) | |
| 20 | g.33438948A>C | CA313275668 | SNTA1 | c.389T>G (p.Phe130Cys) n.622T>G c.62T>G (p.Phe21Cys) | dbSNP gnomAD v3 gnomAD v4 |
| 20 | g.33438948A>G | CA408633516 | SNTA1 | c.389T>C (p.Phe130Ser) n.622T>C c.62T>C (p.Phe21Ser) | gnomAD v4 |
| 20 | g.33438948A>T | CA408633515 | SNTA1 | c.389T>A (p.Phe130Tyr) n.622T>A c.62T>A (p.Phe21Tyr) | |
| 20 | g.33438949A= | CA2360753096 | SNTA1 | c.388T= (p.Phe130=) n.621T= c.61T= (p.Phe21=) | |
| 20 | g.33438949A>C | CA408633517 | SNTA1 | c.388T>G (p.Phe130Val) n.621T>G c.61T>G (p.Phe21Val) | |
| 20 | g.33438949A>G | CA302315 | SNTA1 | c.388T>C (p.Phe130Leu) n.621T>C c.61T>C (p.Phe21Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 20 | g.33438949A>T | CA408633518 | SNTA1 | c.388T>A (p.Phe130Ile) n.621T>A c.61T>A (p.Phe21Ile) | |
| 20 | g.33438950A>C | CA510252240 | SNTA1 | c.387T>G (p.Leu129=) n.620T>G c.60T>G (p.Leu20=) | |
| 20 | g.33438950A>G | CA510252242 | SNTA1 | c.387T>C (p.Leu129=) n.620T>C c.60T>C (p.Leu20=) | |
| 20 | g.33438950A>T | CA510252244 | SNTA1 | c.387T>A (p.Leu129=) n.620T>A c.60T>A (p.Leu20=) | |
| 20 | g.33438951A= | CA2360753097 | SNTA1 | c.386T= (p.Leu129=) n.619T= c.59T= (p.Leu20=) | |
| 20 | g.33438951A>C | CA408633519 | SNTA1 | c.386T>G (p.Leu129Arg) n.619T>G c.59T>G (p.Leu20Arg) | |
| 20 | g.33438951A>G | CA408633520 | SNTA1 | c.386T>C (p.Leu129Pro) n.619T>C c.59T>C (p.Leu20Pro) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 20 | g.33438951A>T | CA408633521 | SNTA1 | c.386T>A (p.Leu129His) n.619T>A c.59T>A (p.Leu20His) | |
| 20 | g.33438952G>A | CA408633522 | SNTA1 | c.385C>T (p.Leu129Phe) n.618C>T c.58C>T (p.Leu20Phe) | |
| 20 | g.33438952G>C | CA408633523 | SNTA1 | c.385C>G (p.Leu129Val) n.618C>G c.58C>G (p.Leu20Val) | |
| 20 | g.33438952G>T | CA408633524 | SNTA1 | c.385C>A (p.Leu129Ile) n.618C>A c.58C>A (p.Leu20Ile) | |
| 20 | g.33438953G>A | CA510252245 | SNTA1 | c.384C>T (p.Ala128=) n.617C>T c.57C>T (p.Ala19=) | gnomAD v4 |
| 20 | g.33438953G>C | CA510252246 | SNTA1 | c.384C>G (p.Ala128=) n.617C>G c.57C>G (p.Ala19=) | gnomAD v4 |
| 20 | g.33438953G>T | CA510252248 | SNTA1 | c.384C>A (p.Ala128=) n.617C>A c.57C>A (p.Ala19=) | |
| 20 | g.33438954G>A | CA408633525 | SNTA1 | c.383C>T (p.Ala128Val) n.616C>T c.56C>T (p.Ala19Val) | |
| 20 | g.33438954G>C | CA408633526 | SNTA1 | c.383C>G (p.Ala128Gly) n.616C>G c.56C>G (p.Ala19Gly) | |
| 20 | g.33438954G>T | CA408633527 | SNTA1 | c.383C>A (p.Ala128Asp) n.616C>A c.56C>A (p.Ala19Asp) | |
| 20 | g.33438955C>A | CA408633528 | SNTA1 | c.382G>T (p.Ala128Ser) n.615G>T c.55G>T (p.Ala19Ser) | |
| 20 | g.33438955C>G | CA408633529 | SNTA1 | c.382G>C (p.Ala128Pro) n.615G>C c.55G>C (p.Ala19Pro) | |
| 20 | g.33438955C>T | CA408633530 | SNTA1 | c.382G>A (p.Ala128Thr) n.615G>A c.55G>A (p.Ala19Thr) | |
| 20 | g.33438956C>A | CA408633532 | SNTA1 | c.381G>T (p.Glu127Asp) n.614G>T c.54G>T (p.Glu18Asp) | |
| 20 | g.33438956C>G | CA408633531 | SNTA1 | c.381G>C (p.Glu127Asp) n.614G>C c.54G>C (p.Glu18Asp) | |
| 20 | g.33438956C>T | CA510252250 | SNTA1 | c.381G>A (p.Glu127=) n.614G>A c.54G>A (p.Glu18=) | gnomAD v4 |
| 20 | g.33438957T>A | CA408633533 | SNTA1 | c.380A>T (p.Glu127Val) n.613A>T c.53A>T (p.Glu18Val) | |
| 20 | g.33438957T>C | CA408633534 | SNTA1 | c.380A>G (p.Glu127Gly) n.613A>G c.53A>G (p.Glu18Gly) | |
| 20 | g.33438957T>G | CA408633535 | SNTA1 | c.380A>C (p.Glu127Ala) n.613A>C c.53A>C (p.Glu18Ala) | |
| 20 | g.33438961_33438964del | CA2652478042 | SNTA1 | c.377_380del (p.Thr126ArgfsTer12) n.610_613del c.50_53del (p.Thr17ArgfsTer12) | gnomAD v4 |
| 20 | g.33438958C>A | CA408633536 | SNTA1 | c.379G>T (p.Glu127Ter) n.612G>T c.52G>T (p.Glu18Ter) | |
| 20 | g.33438958C>G | CA408633537 | SNTA1 | c.379G>C (p.Glu127Gln) n.612G>C c.52G>C (p.Glu18Gln) | |
| 20 | g.33438958C>T | CA408633538 | SNTA1 | c.379G>A (p.Glu127Lys) n.612G>A c.52G>A (p.Glu18Lys) | |
| 20 | g.33438959T>A | CA510252251 | SNTA1 | c.378A>T (p.Thr126=) n.611A>T c.51A>T (p.Thr17=) | |
| 20 | g.33438959T>C | CA510252252 | SNTA1 | c.378A>G (p.Thr126=) n.611A>G c.51A>G (p.Thr17=) | dbSNP gnomAD v2 gnomAD v4 |
| 20 | g.33438959T>G | CA510252254 | SNTA1 | c.378A>C (p.Thr126=) n.611A>C c.51A>C (p.Thr17=) | |
| 20 | g.33438959T= | CA2360753098 | SNTA1 | c.378A= (p.Thr126=) n.611A= c.51A= (p.Thr17=) | |
| 20 | g.33438960G>A | CA408633539 | SNTA1 | c.377C>T (p.Thr126Ile) n.610C>T c.50C>T (p.Thr17Ile) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 20 | g.33438960G>C | CA408633540 | SNTA1 | c.377C>G (p.Thr126Arg) n.610C>G c.50C>G (p.Thr17Arg) | |
| 20 | g.33438960G= | CA2360753099 | SNTA1 | c.377C= (p.Thr126=) n.610C= c.50C= (p.Thr17=) | |
| 20 | g.33438960G>T | CA408633541 | SNTA1 | c.377C>A (p.Thr126Lys) n.610C>A c.50C>A (p.Thr17Lys) | |
| 20 | g.33438961T>A | CA408633542 | SNTA1 | c.376A>T (p.Thr126Ser) n.609A>T c.49A>T (p.Thr17Ser) | |
| 20 | g.33438961T>C | CA408633543 | SNTA1 | c.376A>G (p.Thr126Ala) n.609A>G c.49A>G (p.Thr17Ala) | |
| 20 | g.33438961T>G | CA408633544 | SNTA1 | c.376A>C (p.Thr126Pro) n.609A>C c.49A>C (p.Thr17Pro) | |
| 20 | g.33438962C>A | CA408633545 | SNTA1 | c.375G>T (p.Gln125His) n.608G>T c.48G>T (p.Gln16His) | |
| 20 | g.33438962C= | CA2360753100 | SNTA1 | c.375G= (p.Gln125=) n.608G= c.48G= (p.Gln16=) | |
| 20 | g.33438962C>G | CA236849 | SNTA1 | c.375G>C (p.Gln125His) n.608G>C c.48G>C (p.Gln16His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 20 | g.33438962C>T | CA510252256 | SNTA1 | c.375G>A (p.Gln125=) n.608G>A c.48G>A (p.Gln16=) | COSMIC |
| 20 | g.33438963T>A | CA408633546 | SNTA1 | c.374A>T (p.Gln125Leu) n.607A>T c.47A>T (p.Gln16Leu) | |
| 20 | g.33438963T>C | CA408633548 | SNTA1 | c.374A>G (p.Gln125Arg) n.607A>G c.47A>G (p.Gln16Arg) | |
| 20 | g.33438963T>G | CA408633547 | SNTA1 | c.374A>C (p.Gln125Pro) n.607A>C c.47A>C (p.Gln16Pro) | dbSNP gnomAD v3 gnomAD v4 |
| 20 | g.33438963T= | CA2360753101 | SNTA1 | c.374A= (p.Gln125=) n.607A= c.47A= (p.Gln16=) | |
| 20 | g.33438964G>A | CA408633549 | SNTA1 | c.373C>T (p.Gln125Ter) n.606C>T c.46C>T (p.Gln16Ter) | |
| 20 | g.33438964G>C | CA408633550 | SNTA1 | c.373C>G (p.Gln125Glu) n.606C>G c.46C>G (p.Gln16Glu) | |
| 20 | g.33438964G>T | CA408633551 | SNTA1 | c.373C>A (p.Gln125Lys) n.606C>A c.46C>A (p.Gln16Lys) | |
| 20 | g.33438965G>A | CA510252258 | SNTA1 | c.372C>T (p.Asp124=) n.605C>T c.45C>T (p.Asp15=) | COSMIC |
| 20 | g.33438965G>C | CA408633552 | SNTA1 | c.372C>G (p.Asp124Glu) n.605C>G c.45C>G (p.Asp15Glu) | |
| 20 | g.33438965G>T | CA408633553 | SNTA1 | c.372C>A (p.Asp124Glu) n.605C>A c.45C>A (p.Asp15Glu) | |
| 20 | g.33438966T>A | CA408633554 | SNTA1 | c.371A>T (p.Asp124Val) n.604A>T c.44A>T (p.Asp15Val) | |
| 20 | g.33438966T>C | CA408633555 | SNTA1 | c.371A>G (p.Asp124Gly) n.604A>G c.44A>G (p.Asp15Gly) | |
| 20 | g.33438966T>G | CA408633556 | SNTA1 | c.371A>C (p.Asp124Ala) n.604A>C c.44A>C (p.Asp15Ala) | |
| 20 | g.33438967C>A | CA408633557 | SNTA1 | c.370G>T (p.Asp124Tyr) n.603G>T c.43G>T (p.Asp15Tyr) | |
| 20 | g.33438967C= | CA2360753102 | SNTA1 | c.370G= (p.Asp124=) n.603G= c.43G= (p.Asp15=) | |
| 20 | g.33438967C>G | CA408633558 | SNTA1 | c.370G>C (p.Asp124His) n.603G>C c.43G>C (p.Asp15His) | |
| 20 | g.33438967C>T | CA408633559 | SNTA1 | c.370G>A (p.Asp124Asn) n.603G>A c.43G>A (p.Asp15Asn) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 20 | g.33438968A>C | CA510252261 | SNTA1 | c.369T>G (p.Ala123=) n.602T>G c.42T>G (p.Ala14=) | |
| 20 | g.33438968A>G | CA510252263 | SNTA1 | c.369T>C (p.Ala123=) n.602T>C c.42T>C (p.Ala14=) | gnomAD v4 |
| 20 | g.33438968A>T | CA510252264 | SNTA1 | c.369T>A (p.Ala123=) n.602T>A c.42T>A (p.Ala14=) | |
| 20 | g.33438969G>A | CA408633561 | SNTA1 | c.368C>T (p.Ala123Val) n.601C>T c.41C>T (p.Ala14Val) | |
| 20 | g.33438969G>C | CA408633560 | SNTA1 | c.368C>G (p.Ala123Gly) n.601C>G c.41C>G (p.Ala14Gly) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 20 | g.33438969G= | CA2360753103 | SNTA1 | c.368C= (p.Ala123=) n.601C= c.41C= (p.Ala14=) | |
| 20 | g.33438969G>T | CA9817233 | SNTA1 | c.368C>A (p.Ala123Asp) n.601C>A c.41C>A (p.Ala14Asp) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 20 | g.33438971_33438973del | CA2531311661 | SNTA1 | c.366_368del (p.Ala123del) n.599_601del c.39_41del (p.Ala14del) | |
| 20 | g.33438970C>A | CA408633562 | SNTA1 | c.367G>T (p.Ala123Ser) n.600G>T c.40G>T (p.Ala14Ser) | |
| 20 | g.33438970C>G | CA408633563 | SNTA1 | c.367G>C (p.Ala123Pro) n.600G>C c.40G>C (p.Ala14Pro) | |
| 20 | g.33438970C>T | CA408633564 | SNTA1 | c.367G>A (p.Ala123Thr) n.600G>A c.40G>A (p.Ala14Thr) | |
| 20 | g.33438971T>A | CA510252268 | SNTA1 | c.366A>T (p.Ala122=) n.599A>T c.39A>T (p.Ala13=) | |
| 20 | g.33438971T>C | CA510252269 | SNTA1 | c.366A>G (p.Ala122=) n.599A>G c.39A>G (p.Ala13=) | |
| 20 | g.33438971T>G | CA9817234 | SNTA1 | c.366A>C (p.Ala122=) n.599A>C c.39A>C (p.Ala13=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 20 | g.33438971T= | CA2360753104 | SNTA1 | c.366A= (p.Ala122=) n.599A= c.39A= (p.Ala13=) | |
| 20 | g.33438972G>A | CA408633565 | SNTA1 | c.365C>T (p.Ala122Val) n.598C>T c.38C>T (p.Ala13Val) | |
| 20 | g.33438972G>C | CA408633566 | SNTA1 | c.365C>G (p.Ala122Gly) n.598C>G c.38C>G (p.Ala13Gly) | |
| 20 | g.33438972G>T | CA408633567 | SNTA1 | c.365C>A (p.Ala122Glu) n.598C>A c.38C>A (p.Ala13Glu) | dbSNP gnomAD v3 gnomAD v4 |
| 20 | g.33438973C>A | CA408633568 | SNTA1 | c.364G>T (p.Ala122Ser) n.597G>T c.37G>T (p.Ala13Ser) | |
| 20 | g.33438973C= | CA2360753105 | SNTA1 | c.364G= (p.Ala122=) n.597G= c.37G= (p.Ala13=) | |
| 20 | g.33438973C>G | CA408633569 | SNTA1 | c.364G>C (p.Ala122Pro) n.597G>C c.37G>C (p.Ala13Pro) | |
| 20 | g.33438973C>T | CA302312 | SNTA1 | c.364G>A (p.Ala122Thr) n.597G>A c.37G>A (p.Ala13Thr) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 20 | g.33438974C>A | CA408633570 | SNTA1 | c.363G>T (p.Leu121Phe) n.596G>T c.36G>T (p.Leu12Phe) | |
| 20 | g.33438974C>G | CA408633571 | SNTA1 | c.363G>C (p.Leu121Phe) n.596G>C c.36G>C (p.Leu12Phe) | |
| 20 | g.33438974C>T | CA510252271 | SNTA1 | c.363G>A (p.Leu121=) n.596G>A c.36G>A (p.Leu12=) | |
| 20 | g.33438975A>C | CA408633574 | SNTA1 | c.362T>G (p.Leu121Trp) n.595T>G c.35T>G (p.Leu12Trp) | |
| 20 | g.33438975A>G | CA408633572 | SNTA1 | c.362T>C (p.Leu121Ser) n.595T>C c.35T>C (p.Leu12Ser) | |
| 20 | g.33438975A>T | CA408633573 | SNTA1 | c.362T>A (p.Leu121Ter) n.595T>A c.35T>A (p.Leu12Ter) | |
| 20 | g.33438976A= | CA2360753106 | SNTA1 | c.361T= (p.Leu121=) n.594T= c.34T= (p.Leu12=) | |
| 20 | g.33438976A>C | CA408633575 | SNTA1 | c.361T>G (p.Leu121Val) n.594T>G c.34T>G (p.Leu12Val) | |
| 20 | g.33438976A>G | CA9817235 | SNTA1 | c.361T>C (p.Leu121=) n.594T>C c.34T>C (p.Leu12=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 20 | g.33438976A>T | CA408633576 | SNTA1 | c.361T>A (p.Leu121Met) n.594T>A c.34T>A (p.Leu12Met) | |
| 20 | g.33438977T>A | CA510252275 | SNTA1 | c.360A>T (p.Gly120=) n.593A>T c.33A>T (p.Gly11=) | |
| 20 | g.33438977T>C | CA510252274 | SNTA1 | c.360A>G (p.Gly120=) n.593A>G c.33A>G (p.Gly11=) | |
| 20 | g.33438977T>G | CA510252272 | SNTA1 | c.360A>C (p.Gly120=) n.593A>C c.33A>C (p.Gly11=) | |
| 20 | g.33438978C>A | CA408633577 | SNTA1 | c.359G>T (p.Gly120Val) n.592G>T c.32G>T (p.Gly11Val) | dbSNP gnomAD v3 gnomAD v4 |
| 20 | g.33438978C= | CA2360753107 | SNTA1 | c.359G= (p.Gly120=) n.592G= c.32G= (p.Gly11=) | |
| 20 | g.33438978C>G | CA408633579 | SNTA1 | c.359G>C (p.Gly120Ala) n.592G>C c.32G>C (p.Gly11Ala) | |
| 20 | g.33438978C>T | CA408633578 | SNTA1 | c.359G>A (p.Gly120Glu) n.592G>A c.32G>A (p.Gly11Glu) | |
| 20 | g.33438979C>A | CA408633580 | SNTA1 | c.358G>T (p.Gly120Ter) n.591G>T c.31G>T (p.Gly11Ter) | |
| 20 | g.33438979C>G | CA408633581 | SNTA1 | c.358G>C (p.Gly120Arg) n.591G>C c.31G>C (p.Gly11Arg) | |
| 20 | g.33438979C>T | CA408633582 | SNTA1 | c.358G>A (p.Gly120Arg) n.591G>A c.31G>A (p.Gly11Arg) | |
| 20 | g.33438980C>A | CA408633583 | SNTA1 | c.357G>T (p.Lys119Asn) n.590G>T c.30G>T (p.Lys10Asn) | |
| 20 | g.33438980C>G | CA408633584 | SNTA1 | c.357G>C (p.Lys119Asn) n.590G>C c.30G>C (p.Lys10Asn) | |
| 20 | g.33438980C>T | CA510252277 | SNTA1 | c.357G>A (p.Lys119=) n.590G>A c.30G>A (p.Lys10=) | |
| 20 | g.33438981T>A | CA408633585 | SNTA1 | c.356A>T (p.Lys119Met) n.589A>T c.29A>T (p.Lys10Met) | |
| 20 | g.33438981T>C | CA408633586 | SNTA1 | c.356A>G (p.Lys119Arg) n.589A>G c.29A>G (p.Lys10Arg) | |
| 20 | g.33438981T>G | CA408633587 | SNTA1 | c.356A>C (p.Lys119Thr) n.589A>C c.29A>C (p.Lys10Thr) | |
| 20 | g.33438982T>A | CA408633588 | SNTA1 | c.355A>T (p.Lys119Ter) n.588A>T c.28A>T (p.Lys10Ter) | |
| 20 | g.33438982T>C | CA408633589 | SNTA1 | c.355A>G (p.Lys119Glu) n.588A>G c.28A>G (p.Lys10Glu) | |
| 20 | g.33438982T>G | CA408633590 | SNTA1 | c.355A>C (p.Lys119Gln) n.588A>C c.28A>C (p.Lys10Gln) | |
| 20 | g.33438983G>A | CA510252278 | SNTA1 | c.354C>T (p.Phe118=) n.587C>T c.27C>T (p.Phe9=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 20 | g.33438983G>C | CA408633591 | SNTA1 | c.354C>G (p.Phe118Leu) n.587C>G c.27C>G (p.Phe9Leu) | |
| 20 | g.33438983G= | CA2360753108 | SNTA1 | c.354C= (p.Phe118=) n.587C= c.27C= (p.Phe9=) | |
| 20 | g.33438983G>T | CA408633592 | SNTA1 | c.354C>A (p.Phe118Leu) n.587C>A c.27C>A (p.Phe9Leu) | |
| 20 | g.33438984A= | CA2360753109 | SNTA1 | c.353T= (p.Phe118=) n.586T= c.26T= (p.Phe9=) | |
| 20 | g.33438984A>C | CA408633593 | SNTA1 | c.353T>G (p.Phe118Cys) n.586T>G c.26T>G (p.Phe9Cys) | dbSNP gnomAD v2 gnomAD v4 |
| 20 | g.33438984A>G | CA408633595 | SNTA1 | c.353T>C (p.Phe118Ser) n.586T>C c.26T>C (p.Phe9Ser) | |
| 20 | g.33438984A>T | CA408633594 | SNTA1 | c.353T>A (p.Phe118Tyr) n.586T>A c.26T>A (p.Phe9Tyr) | |
| 20 | g.33438985A>C | CA408633596 | SNTA1 | c.352T>G (p.Phe118Val) n.585T>G c.25T>G (p.Phe9Val) | |
| 20 | g.33438985A>G | CA408633597 | SNTA1 | c.352T>C (p.Phe118Leu) n.585T>C c.25T>C (p.Phe9Leu) | |
| 20 | g.33438985A>T | CA408633598 | SNTA1 | c.352T>A (p.Phe118Ile) n.585T>A c.25T>A (p.Phe9Ile) | |
| 20 | g.33438986G>A | CA510252282 | SNTA1 | c.351C>T (p.Ile117=) n.584C>T c.24C>T (p.Ile8=) | |
| 20 | g.33438986G>C | CA408633599 | SNTA1 | c.351C>G (p.Ile117Met) n.584C>G c.24C>G (p.Ile8Met) | |
| 20 | g.33438986G>T | CA510252280 | SNTA1 | c.351C>A (p.Ile117=) n.584C>A c.24C>A (p.Ile8=) | |
| 20 | g.33438987A>C | CA408633600 | SNTA1 | c.350T>G (p.Ile117Ser) n.583T>G c.23T>G (p.Ile8Ser) | |
| 20 | g.33438987A>G | CA408633601 | SNTA1 | c.350T>C (p.Ile117Thr) n.583T>C c.23T>C (p.Ile8Thr) | |
| 20 | g.33438987A>T | CA408633602 | SNTA1 | c.350T>A (p.Ile117Asn) n.583T>A c.23T>A (p.Ile8Asn) | |
| 20 | g.33438988T>A | CA408633603 | SNTA1 | c.349A>T (p.Ile117Phe) n.582A>T c.22A>T (p.Ile8Phe) | |
| 20 | g.33438988T>C | CA408633604 | SNTA1 | c.349A>G (p.Ile117Val) n.582A>G c.22A>G (p.Ile8Val) | ClinVar dbSNP |
| 20 | g.33438988T>G | CA408633605 | SNTA1 | c.349A>C (p.Ile117Leu) n.582A>C c.22A>C (p.Ile8Leu) | |
| 20 | g.33438989C>A | CA408633606 | SNTA1 | c.348G>T (p.Lys116Asn) n.581G>T c.21G>T (p.Lys7Asn) | gnomAD v4 |
| 20 | g.33438989C>G | CA408633607 | SNTA1 | c.348G>C (p.Lys116Asn) n.581G>C c.21G>C (p.Lys7Asn) | |
| 20 | g.33438989C>T | CA510252283 | SNTA1 | c.348G>A (p.Lys116=) n.581G>A c.21G>A (p.Lys7=) | |
| 20 | g.33438990T>A | CA408633608 | SNTA1 | c.347A>T (p.Lys116Met) n.580A>T c.20A>T (p.Lys7Met) | |
| 20 | g.33438990T>C | CA408633609 | SNTA1 | c.347A>G (p.Lys116Arg) n.580A>G c.20A>G (p.Lys7Arg) | gnomAD v4 |
| 20 | g.33438990T>G | CA408633610 | SNTA1 | c.347A>C (p.Lys116Thr) n.580A>C c.20A>C (p.Lys7Thr) | dbSNP gnomAD v2 gnomAD v4 |
| 20 | g.33438990T= | CA2360753110 | SNTA1 | c.347A= (p.Lys116=) n.580A= c.20A= (p.Lys7=) | |
| 20 | g.33438991T>A | CA408633611 | SNTA1 | c.346A>T (p.Lys116Ter) n.579A>T c.19A>T (p.Lys7Ter) | |
| 20 | g.33438991T>C | CA9817236 | SNTA1 | c.346A>G (p.Lys116Glu) n.579A>G c.19A>G (p.Lys7Glu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 20 | g.33438991T>G | CA408633612 | SNTA1 | c.346A>C (p.Lys116Gln) n.579A>C c.19A>C (p.Lys7Gln) | |
| 20 | g.33438991T= | CA2360753111 | SNTA1 | c.346A= (p.Lys116=) n.579A= c.19A= (p.Lys7=) | |
| 20 | g.33438992G>A | CA510252285 | SNTA1 | c.345C>T (p.Ser115=) n.578C>T c.18C>T (p.Ser6=) | dbSNP |
| 20 | g.33438992G>C | CA510252286 | SNTA1 | c.345C>G (p.Ser115=) n.578C>G c.18C>G (p.Ser6=) | |
| 20 | g.33438992G= | CA2360753112 | SNTA1 | c.345C= (p.Ser115=) n.578C= c.18C= (p.Ser6=) | |
| 20 | g.33438992G>T | CA510252287 | SNTA1 | c.345C>A (p.Ser115=) n.578C>A c.18C>A (p.Ser6=) | |
| 20 | g.33438993G>A | CA408633613 | SNTA1 | c.344C>T (p.Ser115Phe) n.577C>T c.17C>T (p.Ser6Phe) | |
| 20 | g.33438993G>C | CA408633614 | SNTA1 | c.344C>G (p.Ser115Cys) n.577C>G c.17C>G (p.Ser6Cys) | |
| 20 | g.33438993G= | CA2360753113 | SNTA1 | c.344C= (p.Ser115=) n.577C= c.17C= (p.Ser6=) | |
| 20 | g.33438993G>T | CA408633615 | SNTA1 | c.344C>A (p.Ser115Tyr) n.577C>A c.17C>A (p.Ser6Tyr) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 20 | g.33438994A>C | CA408633616 | SNTA1 | c.343T>G (p.Ser115Ala) n.576T>G c.16T>G (p.Ser6Ala) | |
| 20 | g.33438994A>G | CA408633617 | SNTA1 | c.343T>C (p.Ser115Pro) n.576T>C c.16T>C (p.Ser6Pro) | |
| 20 | g.33438994A>T | CA408633618 | SNTA1 | c.343T>A (p.Ser115Thr) n.576T>A c.16T>A (p.Ser6Thr) | |
| 20 | g.33438995A>C | CA408633619 | SNTA1 | c.342T>G (p.Ile114Met) n.575T>G c.15T>G (p.Ile5Met) | |
| 20 | g.33438995A>G | CA510252290 | SNTA1 | c.342T>C (p.Ile114=) n.575T>C c.15T>C (p.Ile5=) | |
| 20 | g.33438995A>T | CA510252291 | SNTA1 | c.342T>A (p.Ile114=) n.575T>A c.15T>A (p.Ile5=) |