Original source

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

Alleles
C/A/G/T | Ancestral: C | Ambiguity code: N | MAF: 0.11 (T)
Location

Chromosome 2:241808314 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM093783, CM910014, CD073566

Most severe consequence
Evidence status

Clinical significance

This variation has 5 synonyms - click the plus to show

This variation has 12 HGVS names - click the plus to show

Variant allele A
2:g.241808314C>A
ENST00000472436.1:n.52C>A
ENST00000307503.3:c.32C>A
ENSP00000302620.3:p.Pro11His

Variant allele T
2:g.241808314C>T
ENST00000472436.1:n.52C>T
ENST00000307503.3:c.32C>T
ENSP00000302620.3:p.Pro11Leu

Variant allele G
2:g.241808314C>G
ENST00000472436.1:n.52C>G
ENST00000307503.3:c.32C>G
ENSP00000302620.3:p.Pro11Arg

Genotyping chips

This variation has assays on: Illumina_ExomeChip, Illumina_HumanOmni1-Quad, Illumina_HumanOmni5

Variation displays