| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000240328 |
| Start |
61408342:61408342(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1975C>G |
| AA Mutation |
p.Leu659Val(p.L659V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000240328 |
| Start |
61401751:61401751(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.463A>T |
| AA Mutation |
p.Met155Leu(p.M155L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000240328 |
| Start |
61408284:61408284(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs768086181
|
| CDS Mutation |
c.1917C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |