| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000307751 |
| Start |
38803536:38803536(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.556C>A |
| AA Mutation |
p.Pro186Thr(p.P186T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000307751 |
| Start |
38812485:38812485(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.80T>C |
| AA Mutation |
p.Leu27Pro(p.L27P) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000307751 |
| Start |
38802073:38802073(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.744G>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |