ENU mutagenesis induced an A-to-G transition at base pair 71,683,377 (GRCm38) on chromosome 8, or base pair 6,995 in the GenBank genomic region NC_000074. The mutation corresponds to residue 2,030 in the mRNA sequence NM_010589 within exon 14 of 25 total exons. The mutation results in a tyrosine (Y) to cysteine (C) substitution at position 607 (p.Y607C). (J:217795)
Legend:
cx: complex: > 1 genome feature ot: other: hemizygous, indeterminate,... (F): Female
(M): Male
N: normal phenotype
(#): related diseases count