Colon Cancer: Gene >> EFNA5
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000333274 |
| Start |
107381262:107381262(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs767938203
|
| CDS Mutation |
c.680C>T |
| AA Mutation |
p.Thr227Ile(p.T227I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000333274 |
| Start |
107381298:107381298(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.644T>C |
| AA Mutation |
p.Leu215Ser(p.L215S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> EFNA5
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000333274 |
| Start |
107387283:107387283(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.517C>T |
| AA Mutation |
p.Arg173Cys(p.R173C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000333274 |
| Start |
107427261:107427261(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.374C>T |
| AA Mutation |
p.Ser125Phe(p.S125F) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000333274 |
| Start |
107427364:107427364(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs780608946
|
| CDS Mutation |
c.271G>A |
| AA Mutation |
p.Asp91Asn(p.D91N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000333274 |
| Start |
107670599:107670599(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.15G>T |
| AA Mutation |
p.Glu5Asp(p.E5D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000333274 |
| Start |
107427301:107427301(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.334C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| Mutation ID |
6 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000333274 |
| Start |
107387722:107387722(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.468C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
|