Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K | MAF: < 0.01 (G)
Location

Chromosome 12:101830666 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM060284

Most severe consequence
Evidence status

Clinical significance

This variation has 4 synonyms - click the plus to show

This variation has 9 HGVS names - click the plus to show

12:g.101830666T>G
ENST00000549940.2:c.10A>C
ENSP00000449150.1:p.Lys4Gln
ENST00000392919.4:c.10A>C
ENSP00000376651.4:p.Lys4Gln
ENST00000549165.1:c.10A>C
ENSP00000450413.1:p.Lys4Gln
ENST00000299314.8:c.10A>C
ENSP00000299314.7:p.Lys4Gln

Variation displays