Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
T/A | Ancestral: T | Ambiguity code: W
Location

Chromosome 11:57614439 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM920132 ; PhenCode SERPING1base_D0077:g.17935T>A (T/A)

Most severe consequence
Clinical significance

Synonyms

LSDB 14189

This variation has 19 HGVS names - click the plus to show

11:g.57614439T>A
ENST00000278407.6:c.1361T>A
ENSP00000278407.4:p.Val454Glu
ENST00000528996.1:c.*301T>A
ENST00000531797.3:c.*386T>A
ENST00000403558.1:c.1490T>A
ENSP00000384420.1:p.Val497Glu
ENST00000530113.1:n.818T>A
ENST00000619430.1:c.*90T>A
ENST00000378324.4:c.1205T>A
ENSP00000367575.2:p.Val402Glu
ENST00000340687.8:c.1250T>A
ENSP00000341861.6:p.Val417Glu
ENST00000531133.3:c.*730T>A
ENST00000378323.6:c.1376T>A
ENSP00000367574.4:p.Val459Glu
LRG_105:g.21886T>A
LRG_105t1:c.1361T>A
LRG_105p1:p.Val454Glu

Variation displays