| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000400324 |
| Start |
60042780:60042780(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.536T>C |
| AA Mutation |
p.Phe179Ser(p.F179S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000400324 |
| Start |
59924809:59924809(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.2136T>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000400324 |
| Start |
59969963:59969963(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2055A>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |