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SNP ID Transcript ID Gene Name: Consequence Type BioType Protein ID Protein Position Residue Change
cfa1166255 ENSCAFT00000093797 ENSCAFG00000000338:NMD_transcript_variant protein_coding ENSCAFP00000057788 - -
cfa1166256 ENSCAFT00000000528 ENSCAFG00000000338:NMD_transcript_variant protein_coding ENSCAFP00000000479 - -
cfa1166256 ENSCAFT00000093797 ENSCAFG00000000338:NMD_transcript_variant protein_coding ENSCAFP00000057788 - -
cfa1166257 ENSCAFT00000000528 ENSCAFG00000000338:NMD_transcript_variant protein_coding ENSCAFP00000000479 - -
cfa1166257 ENSCAFT00000093797 ENSCAFG00000000338:NMD_transcript_variant protein_coding ENSCAFP00000057788 - -
cfa1166258 ENSCAFT00000000528 ENSCAFG00000000338:NMD_transcript_variant protein_coding ENSCAFP00000000479 - -
cfa1166258 ENSCAFT00000093797 ENSCAFG00000000338:NMD_transcript_variant protein_coding ENSCAFP00000057788 - -
cfa1166259 ENSCAFT00000000528 ENSCAFG00000000338:NMD_transcript_variant protein_coding ENSCAFP00000000479 - -
cfa1166259 ENSCAFT00000093797 ENSCAFG00000000338:NMD_transcript_variant protein_coding ENSCAFP00000057788 - -
cfa1166260 ENSCAFT00000000528 ENSCAFG00000000338:NMD_transcript_variant protein_coding ENSCAFP00000000479 - -
cfa1166260 ENSCAFT00000093797 ENSCAFG00000000338:NMD_transcript_variant protein_coding ENSCAFP00000057788 - -
cfa1166261 ENSCAFT00000000528 ENSCAFG00000000338:NMD_transcript_variant protein_coding ENSCAFP00000000479 - -
cfa1166261 ENSCAFT00000093797 ENSCAFG00000000338:NMD_transcript_variant protein_coding ENSCAFP00000057788 - -
cfa1166262 ENSCAFT00000000528 ENSCAFG00000000338:NMD_transcript_variant protein_coding ENSCAFP00000000479 - -
cfa1166262 ENSCAFT00000093797 ENSCAFG00000000338:NMD_transcript_variant protein_coding ENSCAFP00000057788 - -