Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

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

Chromosome 16:23646214 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM070241 ; PhenCode PALB2:c.1653T>A (A/T)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 16730, NM_024675.3:c.1653T>A

This variation has 8 HGVS names - click the plus to show

16:g.23646214A>T
ENST00000565038.1:c.86+2957T>A
ENST00000568219.1:c.*1528T>A
ENST00000261584.4:c.1653T>A
ENSP00000261584.4:p.Tyr551Ter
LRG_308:g.11465T>A
LRG_308t1.1:c.1653T>A
LRG_308p1.1:p.Tyr551Ter

Variation displays