| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000414423 |
| Start |
224398217:224398217(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1654T>A |
| AA Mutation |
p.Leu552Ile(p.L552I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000414423 |
| Start |
224398590:224398590(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1569A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000414423 |
| Start |
224433770:224433770(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.336C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |