| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000361902 |
| Start |
28510831:28510831(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.161T>C |
| AA Mutation |
p.Ile54Thr(p.I54T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000361902 |
| Start |
28510845:28510845(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs767523979
|
| CDS Mutation |
c.147C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000361902 |
| Start |
28504442:28504442(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.516G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |