Original source

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

Alleles
C/G/T | Ancestral: C | Ambiguity code: B
Location

Chromosome 11:17387943 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM061826, CM050280

Most severe consequence
Evidence status

Clinical significance

This variation has 6 synonyms - click the plus to show

This variation has 14 HGVS names - click the plus to show

Variant allele T
11:g.17387943C>T
ENST00000528992.1:c.166G>A
ENSP00000436479.1:p.Arg56Gln
ENST00000526912.1:c.-17+75G>A
ENST00000528731.1:c.-16-97G>A
ENST00000339994.4:c.149G>A
ENSP00000345708.4:p.Arg50Gln

Variant allele G
11:g.17387943C>G
ENST00000528992.1:c.166G>C
ENSP00000436479.1:p.Arg56Pro
ENST00000526912.1:c.-17+75G>C
ENST00000528731.1:c.-16-97G>C
ENST00000339994.4:c.149G>C
ENSP00000345708.4:p.Arg50Pro

Variation displays