Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.24 (G)
Location

Chromosome 14:94847415 (forward strand) | View in location tab

Most severe consequence
Evidence status

Clinical significance

This variation has 9 synonyms - click the plus to show

This variation has 21 HGVS names - click the plus to show

14:g.94847415A>G
ENST00000448921.1:c.710T>C
ENSP00000416066.1:p.Val237Ala
ENST00000449399.3:c.710T>C
ENSP00000416354.3:p.Val237Ala
ENST00000355814.4:c.710T>C
ENSP00000348068.4:p.Val237Ala
ENST00000404814.4:c.710T>C
ENSP00000385960.4:p.Val237Ala
ENST00000393088.4:c.710T>C
ENSP00000376803.4:p.Val237Ala
ENST00000393087.4:c.710T>C
ENSP00000376802.4:p.Val237Ala
ENST00000437397.1:c.710T>C
ENSP00000408474.1:p.Val237Ala
ENST00000402629.1:c.710T>C
ENSP00000386094.1:p.Val237Ala
ENST00000489769.1:c.710T>C
ENSP00000451525.1:p.Val237Ala
ENST00000440909.1:c.710T>C
ENSP00000390299.1:p.Val237Ala

This variation has assays on 5 chips - click the plus to show

Variation displays