This variation has been flagged
Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]
Note: The reference sequence for this variant (C) does not match the Ensembl reference sequence (CA) at this location.
Chromosome 15:74719299-74719300 (forward strand) | View in location tab
This variant overlaps 20 transcripts.