Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 14:94849160 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM900183

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 27 HGVS names - click the plus to show

14:g.94849160C>T
ENST00000448921.1:c.415G>A
ENSP00000416066.1:p.Gly139Ser
ENST00000449399.3:c.415G>A
ENSP00000416354.3:p.Gly139Ser
ENST00000554720.1:c.157G>A
ENSP00000450561.1:p.Gly53Ser
ENST00000404814.4:c.415G>A
ENSP00000385960.4:p.Gly139Ser
ENST00000393087.4:c.415G>A
ENSP00000376802.4:p.Gly139Ser
ENST00000437397.1:c.415G>A
ENSP00000408474.1:p.Gly139Ser
ENST00000489769.1:c.415G>A
ENSP00000451525.1:p.Gly139Ser
ENST00000556091.1:c.415G>A
ENSP00000452169.1:p.Gly139Ser
ENST00000355814.4:c.415G>A
ENSP00000348068.4:p.Gly139Ser
ENST00000557492.1:c.415G>A
ENSP00000452452.1:p.Gly139Ser
ENST00000393088.4:c.415G>A
ENSP00000376803.4:p.Gly139Ser
ENST00000402629.1:c.415G>A
ENSP00000386094.1:p.Gly139Ser
ENST00000440909.1:c.415G>A
ENSP00000390299.1:p.Gly139Ser

Variation displays