| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000399410 |
| Start |
16044494:16044494(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.854C>A |
| AA Mutation |
p.Pro285Gln(p.P285Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000399410 |
| Start |
16090456:16090456(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs780819239
|
| CDS Mutation |
c.2512A>G |
| AA Mutation |
p.Ile838Val(p.I838V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000399410 |
| Start |
16045947:16045947(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1152C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |