Coding SNP Information
in DQ2 on chrom 11
ID | SNP ID | Position | Gene Name:SNP Location | SNP Class | Ref | Genotype | Residue Change |
---|---|---|---|---|---|---|---|
1 | snp_cf0010000370752 | Chr11:1963683 | ENSCAFG00000000350:intron ENSCAFG00000000350:CDS | snp | T | C | M => V |
2 | snp_cf0010000370535 | Chr11:388909 | ENSCAFG00000012915:CDS | snp | C | G | P => A |
3 | snp_cf0010000370695 | Chr11:1573374 | ENSCAFG00000000391:CDS ENSCAFG00000000391:intron | snp | G | T | stop_codon => L |
4 | snp_cf0010000370696 | Chr11:1573375 | ENSCAFG00000000391:splice_site ENSCAFG00000000391:CDS | snp | A | G | stop_codon => W |
5 | snp_cf0010000370751 | Chr11:1963682 | ENSCAFG00000000350:intron ENSCAFG00000000350:CDS | snp | A | T | M => K |
6 | snp_cf0010000370536 | Chr11:388954 | ENSCAFG00000012915:CDS | snp | G | T | G => C |
7 | snp_cf0010000370537 | Chr11:388973 | ENSCAFG00000012915:CDS | snp | A | G | N => S |
8 | snp_cf0010000370418 | Chr11:116125 | ENSCAFG00000012938:CDS | snp | T | Y | R => R |
9 | snp_cf0010000370489 | Chr11:197678 | ENSCAFG00000030899:CDS | snp | C | S | S => T |
10 | snp_cf0010000370744 | Chr11:1894459 | ENSCAFG00000000354:CDS | snp | A | G | G => G |