| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000237596 |
| Start |
88038485:88038485(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1078C>T |
| AA Mutation |
p.Pro360Ser(p.P360S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000237596 |
| Start |
88065480:88065480(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2225G>A |
| AA Mutation |
p.Arg742Gln(p.R742Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000237596 |
| Start |
88046864:88046864(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs145716012
|
| CDS Mutation |
c.1542C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |