Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K | MAF: 0.23 (G)
Location

Chromosome 14:94844843 (forward strand) | View in location tab

Co-located

with COSMIC COSM147838 (T/G)

Most severe consequence
Evidence status

Clinical significance

This variation has 8 synonyms - click the plus to show

This variation has 18 HGVS names - click the plus to show

14:g.94844843T>G
ENST00000448921.1:c.1200A>C
ENSP00000416066.1:p.Glu400Asp
ENST00000449399.3:c.1200A>C
ENSP00000416354.3:p.Glu400Asp
ENST00000355814.4:c.1200A>C
ENSP00000348068.4:p.Glu400Asp
ENST00000404814.4:c.1200A>C
ENSP00000385960.4:p.Glu400Asp
ENST00000393088.4:c.1200A>C
ENSP00000376803.4:p.Glu400Asp
ENST00000393087.4:c.1200A>C
ENSP00000376802.4:p.Glu400Asp
ENST00000437397.1:c.1200A>C
ENSP00000408474.1:p.Glu400Asp
ENST00000489769.1:c.*499A>C
ENST00000440909.1:c.1200A>C
ENSP00000390299.1:p.Glu400Asp

This variation has assays on 9 chips - click the plus to show

Variation displays