Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.07 (T)
Location

Chromosome 14:61740839 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM035511

Most severe consequence
Evidence status

This variation has 4 synonyms - click the plus to show

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

14:g.61740839C>T
ENST00000555937.1:n.148+6554C>T
ENST00000539097.2:c.1816C>T
ENSP00000437955.1:p.Pro606Ser
ENST00000554254.1:n.213+10046G>A
ENST00000337138.5:c.1744C>T
ENSP00000338018.4:p.Pro582Ser
ENST00000547430.2:n.652C>T
ENST00000555014.1:n.390C>T
ENST00000323441.7:c.1744C>T
ENSP00000323326.6:p.Pro582Ser
ENST00000557538.2:c.1567C>T
ENSP00000451696.1:p.Pro523Ser
ENST00000394997.2:c.1747C>T
ENSP00000378446.1:p.Pro583Ser

This variation has assays on 10 chips - click the plus to show

Variation displays