| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000361546 |
| Start |
154254043:154254043(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1808C>T |
| AA Mutation |
p.Pro603Leu(p.P603L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000361546 |
| Start |
154253925:154253925(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1690A>T |
| AA Mutation |
p.Asn564Tyr(p.N564Y) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000361546 |
| Start |
154228668:154228668(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.222C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |