Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R
Location

Chromosome 16:88809834 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM880009

Most severe consequence
Evidence status

Clinical significance

This variation has 4 synonyms - click the plus to show

This variation has 13 HGVS names - click the plus to show

16:g.88809834A>G
ENST00000426324.4:c.401-128T>C
ENST00000563655.3:c.326T>C
ENSP00000456012.1:p.Met109Thr
ENST00000562464.1:n.417T>C
ENST00000567713.3:c.322-299T>C
ENST00000378364.5:c.407T>C
ENSP00000367615.3:p.Met136Thr
ENST00000569616.1:c.472T>C
ENST00000567057.3:n.200-128T>C
ENST00000568575.1:n.336T>C
ENST00000567391.3:c.*81T>C
ENST00000568319.3:c.*75-128T>C

Variation displays