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 16:88810141 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM940079

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_010_APRT_102600_0007

This variation has 15 HGVS names - click the plus to show

16:g.88810141A>G
ENST00000426324.3:c.329T>C
ENSP00000397007.2:p.Leu110Pro
ENST00000563655.2:c.248T>C
ENSP00000456012.1:p.Leu83Pro
ENST00000562464.1:n.339T>C
ENST00000567713.2:c.321+282T>C
ENST00000378364.4:c.329T>C
ENSP00000367615.3:p.Leu110Pro
ENST00000567057.2:n.128T>C
ENST00000569616.1:c.327T>C
ENSP00000455692.1:p.Leu110Pro
ENST00000568575.1:n.258T>C
ENST00000567391.2:c.*3T>C
ENST00000568319.2:c.*3T>C

Variation displays