Coding SNP Information
in DQ8 on chrom 12
| ID | SNP ID | Position | Gene Name:SNP Location | SNP Class | Ref | Genotype | Residue Change |
|---|---|---|---|---|---|---|---|
| 1 | snp_cf0016000509410 | Chr12:397101 | ENSCAFG00000030478:CDS | snp | T | W | S => T |
| 2 | snp_cf0016000509498 | Chr12:442727 | ENSCAFG00000000414:CDS | snp | T | C | L => P |
| 3 | snp_cf0016000509455 | Chr12:420732 | ENSCAFG00000000406:CDS | snp | T | Y | T => T |
| 4 | snp_cf0016000509313 | Chr12:332051 | ENSCAFG00000000394:CDS | snp | C | T | R => R |
| 5 | snp_cf0016000508963 | Chr12:121864 | ENSCAFG00000000367:CDS | snp | A | R | I => T |
| 6 | snp_cf0016000509421 | Chr12:401400 | ENSCAFG00000030478:NON_CDS ENSCAFG00000030478:CDS | snp | C | G | L => V |
| 7 | snp_cf0016000509422 | Chr12:401537 | ENSCAFG00000030478:intron ENSCAFG00000030478:CDS | snp | G | K | G => C |
| 8 | snp_cf0016000508933 | Chr12:109419 | ENSCAFG00000000367:CDS | snp | G | R | V => V |
| 9 | snp_cf0016000508934 | Chr12:109435 | ENSCAFG00000000367:CDS | snp | G | R | P => L |
| 10 | snp_cf0016000509182 | Chr12:246636 | ENSCAFG00000000386:CDS | snp | G | R | S => S |