Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M
Location

Chromosome 1:201361988 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM043595

Most severe consequence
Clinical significance

Synonyms

LSDB 5871

This variation has 27 HGVS names - click the plus to show

1:g.201361988C>A
ENST00000491504.3:n.1853G>T
ENST00000367318.7:c.614G>T
ENSP00000356287.5:p.Arg205Leu
ENST00000458432.4:c.428G>T
ENSP00000387874.3:p.Arg143Leu
ENST00000460780.3:n.937G>T
ENST00000367317.6:c.596G>T
ENSP00000356286.5:p.Arg199Leu
ENST00000367315.4:c.623G>T
ENSP00000356284.3:p.Arg208Leu
ENST00000360372.6:c.515G>T
ENSP00000353535.5:p.Arg172Leu
ENST00000509001.3:c.614G>T
ENSP00000422031.1:p.Arg205Leu
ENST00000367322.3:c.605G>T
ENSP00000356291.1:p.Arg202Leu
ENST00000421663.4:c.428G>T
ENSP00000404134.3:p.Arg143Leu
ENST00000476888.3:n.99G>T
ENST00000438742.3:c.596G>T
ENSP00000414036.1:p.Arg199Leu
ENST00000367320.4:c.515G>T
ENSP00000356289.2:p.Arg172Leu
ENST00000515042.3:n.540G>T
ENST00000236918.9:c.644G>T
ENSP00000236918.8:p.Arg215Leu

Variation displays