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. 2016 Mar 31;48:25. doi: 10.1186/s12711-016-0207-z

Table 1.

Ten sequence variants that are compatible with recessive inheritance

Chr Position (bp) NCBI reference ID Type Ref Alt Affected gene Effect
3 15,079,217 rs723240647 Indel C GON4L p.E1430Kfs66
3 15,713,943* rs524337907 SNP G C
3 15,713,959* rs719431247 SNP G A
3 15,737,755* rs723848297 SNP C T
3 15,737,992* ss1457237026 Indel T
3 15,738,245* rs720131431 Indel C
3 15,815,016* rs723370534 SNP G A KCNN3 Intronic
3 15,924,914* rs717718209 SNP G A KCNN3 Intronic
3 16,046,490* rs720952332 SNP T C ADAR Intronic
3 16,131,785 rs715250609 SNP T C TDRD10 Intronic

The chromosomal position (base pairs) of compatible variants was based on the UMD3.1 assembly of the bovine genome. The asterisks indicate eight variants that are polymorphic among 1005 animals from 28 breeds other than Fleckvieh that had been sequenced for the 1000 bull genomes project

Ref reference allele, Alt alternate allele