Original source

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

Alleles
A/G/T | Ancestral: A | Ambiguity code: D
Location

Chromosome 17:39768579 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM013759 ; PhenCode HIFD_KRT16:c.362T>C (A/G), HIFD_KRT16:c.362T>A (A/T)

Most severe consequence
Evidence status

Clinical significance

This variation has 6 synonyms - click the plus to show

This variation has 10 HGVS names - click the plus to show

Variant allele T
17:g.39768579A>T
ENST00000588319.1:n.439T>A
ENST00000593067.1:c.-312-41T>A
ENST00000301653.4:c.362T>A
ENSP00000301653.3:p.Met121Lys

Variant allele G
17:g.39768579A>G
ENST00000588319.1:n.439T>C
ENST00000593067.1:c.-312-41T>C
ENST00000301653.4:c.362T>C
ENSP00000301653.3:p.Met121Thr

Variation displays