| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000307161 |
| Start |
186533759:186533759(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.983C>A |
| AA Mutation |
p.Ala328Asp(p.A328D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000307161 |
| Start |
186534049:186534049(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.693A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000307161 |
| Start |
186534037:186534037(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.705G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |