Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
C/T|Ancestral: C|Ambiguity code: Y|MAF: 0.16 (T)
Location

Chromosome 18:58128734 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 15 HGVS names - Hide

18:g.58128734C>T
ENST00000590694.5:n.92-37054C>T
ENST00000591579.5:n.93-37054C>T
ENST00000585594.5:n.169-37054C>T
ENST00000591989.5:n.101-37058C>T
ENST00000356462.10:c.49-37054C>T
ENST00000592846.5:c.-370-37058C>T
ENST00000588516.5:n.1149-37054C>T
ENST00000589054.5:c.48+84026C>T
ENST00000400345.7:c.49-37054C>T
ENST00000256830.13:c.49-37054C>T
ENST00000585363.5:n.86-37054C>T
ENST00000382850.8:c.49-37054C>T
ENST00000456986.5:c.-315-37054C>T
ENST00000587547.1:n.838-37054C>T

About this variant

This variant overlaps 14 transcripts, has 2756 sample genotypes and is mentioned in 1 citation.

Variant displays