Colon Cancer: Gene >> RAB10
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000264710 |
| Start |
26127898:26127898(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.466A>C |
| AA Mutation |
p.Asn156His(p.N156H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
splice_donor_variant |
| Transcription ID |
ENST00000264710 |
| Start |
26127953:26127953(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.519+2T>C |
| Mutation Classification |
Splice_Site |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> RAB10
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000264710 |
| Start |
26109788:26109788(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.209G>A |
| AA Mutation |
p.Arg70Gln(p.R70Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000264710 |
| Start |
26127868:26127868(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.436A>C |
| AA Mutation |
p.Ile146Leu(p.I146L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|