Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 2:98396755 (forward strand) | View in location tab

Co-located

with COSMIC COSM722741 (G/T), COSM77490 (G/A), COSM1410191 (G/C) ; HGMD-PUBLIC CM980379

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_022_CNGA3_600053_0008, 8883

This variation has 9 HGVS names - click the plus to show

2:g.98396755G>A
ENST00000409937.1:c.1597G>A
ENSP00000386761.1:p.Val533Met
ENST00000436404.3:c.1531G>A
ENSP00000410070.2:p.Val511Met
ENST00000393504.2:c.1585G>A
ENSP00000377140.1:p.Val529Met
ENST00000272602.3:c.1585G>A
ENSP00000272602.2:p.Val529Met

Variation displays