Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 1:201359636 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM043596

Most severe consequence
Clinical significance

Synonyms

LSDB 5872

This variation has 26 HGVS names - click the plus to show

1:g.201359636C>T
ENST00000491504.4:n.2047G>A
ENST00000367318.8:c.808G>A
ENSP00000356287.5:p.Asp270Asn
ENST00000458432.5:c.622G>A
ENSP00000387874.3:p.Asp208Asn
ENST00000460780.4:n.1957G>A
ENST00000367317.7:c.790G>A
ENSP00000356286.5:p.Asp264Asn
ENST00000367315.5:c.817G>A
ENSP00000356284.3:p.Asp273Asn
ENST00000360372.7:c.709G>A
ENSP00000353535.5:p.Asp237Asn
ENST00000509001.4:c.808G>A
ENSP00000422031.1:p.Asp270Asn
ENST00000367322.4:c.799G>A
ENSP00000356291.1:p.Asp267Asn
ENST00000421663.5:c.622G>A
ENSP00000404134.3:p.Asp208Asn
ENST00000476888.4:n.255G>A
ENST00000438742.4:c.790G>A
ENSP00000414036.1:p.Asp264Asn
ENST00000367320.5:c.709G>A
ENSP00000356289.2:p.Asp237Asn
ENST00000236918.10:c.838G>A
ENSP00000236918.8:p.Asp280Asn

About this variant

This variant overlaps 19 transcripts and is associated with 2 phenotypes.

Variation displays