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SNP ID Transcript ID Gene Name: Consequence Type BioType Protein ID Protein Position Residue Change
cfa21168298 ENSCAFT00000027700 ENSCAFG00000017478:NMD_transcript_variant protein_coding ENSCAFP00000025761 - -
cfa21168298 ENSCAFT00000043691 ENSCAFG00000017478:NMD_transcript_variant protein_coding ENSCAFP00000043116 - -
cfa21168298 ENSCAFT00000050179 ENSCAFG00000017478:NMD_transcript_variant protein_coding ENSCAFP00000039614 - -
cfa21168298 ENSCAFT00000070341 ENSCAFG00000017478:NMD_transcript_variant protein_coding ENSCAFP00000064879 - -
cfa21168298 ENSCAFT00000087482 ENSCAFG00000017478:NMD_transcript_variant protein_coding ENSCAFP00000049235 - -
cfa21168299 ENSCAFT00000027700 ENSCAFG00000017478:NMD_transcript_variant protein_coding ENSCAFP00000025761 - -
cfa21168299 ENSCAFT00000043691 ENSCAFG00000017478:NMD_transcript_variant protein_coding ENSCAFP00000043116 - -
cfa21168299 ENSCAFT00000050179 ENSCAFG00000017478:NMD_transcript_variant protein_coding ENSCAFP00000039614 - -
cfa21168299 ENSCAFT00000070341 ENSCAFG00000017478:NMD_transcript_variant protein_coding ENSCAFP00000064879 - -
cfa21168299 ENSCAFT00000087482 ENSCAFG00000017478:NMD_transcript_variant protein_coding ENSCAFP00000049235 - -
cfa21168300 ENSCAFT00000027700 ENSCAFG00000017478:NMD_transcript_variant protein_coding ENSCAFP00000025761 - -
cfa21168300 ENSCAFT00000043691 ENSCAFG00000017478:NMD_transcript_variant protein_coding ENSCAFP00000043116 - -
cfa21168300 ENSCAFT00000050179 ENSCAFG00000017478:NMD_transcript_variant protein_coding ENSCAFP00000039614 - -
cfa21168300 ENSCAFT00000070341 ENSCAFG00000017478:NMD_transcript_variant protein_coding ENSCAFP00000064879 - -
cfa21168300 ENSCAFT00000087482 ENSCAFG00000017478:NMD_transcript_variant protein_coding ENSCAFP00000049235 - -