e.g. 1:1246..9423
Coding SNP Information in FAMBGSD00001 on chrom 9
ID SNP ID Position Gene Name:SNP Location SNP Class Ref Genotype Residue Change
1 snp_cf0019003499578 Chr9:428852 ENSCAFG00000005882:intron ENSCAFG00000005859:CDS ENSCAFG00000005765:intron snp T G H => Q
2 snp_cf0019003499485 Chr9:263310 ENSCAFG00000005933:intron ENSCAFG00000005938:CDS ENSCAFG00000005952:intron snp A G N => N
3 snp_cf0019003499486 Chr9:265767 ENSCAFG00000005952:CDS ENSCAFG00000005933:intron snp T C S => P
4 snp_cf0019003499488 Chr9:269797 ENSCAFG00000005933:CDS snp T C G => G
5 snp_cf0019003499589 Chr9:456802 ENSCAFG00000005765:intron ENSCAFG00000005846:CDS snp G A A => V
6 snp_cf0019003499474 Chr9:242471 ENSCAFG00000005933:intron ENSCAFG00000006006:CDS snp T C G => G
7 snp_cf0019003499410 Chr9:110457 ENSCAFG00000006054:CDS snp T C H => R
8 snp_cf0019003499434 Chr9:164541 ENSCAFG00000006048:CDS ENSCAFG00000005933:intron snp C G A => A
9 snp_cf0019003499511 Chr9:298933 ENSCAFG00000005915:CDS snp G C P => R
10 snp_cf0019003499554 Chr9:356335 ENSCAFG00000005911:CDS ENSCAFG00000005765:intron snp G C G => R