Gene >> BTG2
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000290551 |
| Start |
203307352:203307352(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.391T>G |
| AA Mutation |
p.Ser131Ala(p.S131A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000290551 |
| Start |
203305673:203305673(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.67C>A |
| AA Mutation |
p.Leu23Ile(p.L23I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |