TABLE 6.
SNP genome coordinate | Gene/mRNA affected | Line(s) in which SNP is present | Alleles (ref/SNP) | mRNA base change | Comments |
---|---|---|---|---|---|
Chr1:106631586 | IFNAR1 | 0 a | C/T | C/U | Identified as gga‐miR‐1627‐3p binding site |
Chr1:106632281 | IFNAR1 | 15I, 61, 72, C, N, P2a a , 0, Wl | T/C | U/C | Identified as gga‐miR‐196‐1‐3p binding site |
Chr7:7933106 | STAT1 | 61, C, P2a a , 0 a | C/T | N/A | Identified as V‐MAF TF binding site |
SNP occurs in only one allele and is therefore heterozygous.