Coding SNP Information
in dbSNP139 on chrom 7
ID | SNP ID | Position | Gene Name:SNP Location | SNP Class | Ref | Genotype | Residue Change |
---|---|---|---|---|---|---|---|
1 | snp_cf0003002404448 | Chr7:43408 | ENSCAFG00000010288:CDS | snp | A | G | I => V |
2 | snp_cf0003002404491 | Chr7:180153 | ENSCAFG00000029646:intron ENSCAFG00000010330:CDS | snp | C | T | S => S |
3 | snp_cf0003002404492 | Chr7:180543 | ENSCAFG00000029646:intron ENSCAFG00000010330:CDS | snp | T | A | D => V |
4 | snp_cf0003002404453 | Chr7:46040 | ENSCAFG00000010298:CDS | snp | G | T | P => T |
5 | snp_cf0003002404454 | Chr7:46056 | ENSCAFG00000010298:CDS | snp | A | G | P => P |
6 | snp_cf0003002404493 | Chr7:180585 | ENSCAFG00000029646:CDS | snp | T | A | C => stop_codon |
7 | snp_cf0003002404494 | Chr7:180697 | ENSCAFG00000029646:CDS | snp | G | A | A => T |
8 | snp_cf0003002404495 | Chr7:180718 | ENSCAFG00000029646:CDS | snp | G | A | G => S |
9 | snp_cf0003002404452 | Chr7:46038 | ENSCAFG00000010298:CDS | snp | T | A | P => P |
10 | snp_cf0003002404484 | Chr7:148631 | ENSCAFG00000010321:CDS ENSCAFG00000029646:intron | snp | C | T | E => K |