Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 17:39724744 (forward strand) | View in location tab

Co-located

with COSMIC COSM19875 (G/TTGT), COSM303938 (G/T), COSM12554 (G/CTTT), COSM20895 (G/TTAT), COSM685 (G/A) ; ClinVar rs397516980 (G/TTAT)

Most severe consequence
Evidence status

Clinical significance

This variation has 4 synonyms - click the plus to show

This variation has 17 HGVS names - click the plus to show

17:g.39724744G>A
ENST00000583038.2:n.3460G>A
ENST00000580074.1:c.432G>A
ENSP00000463002.1:p.Gly145Ser
ENST00000584450.2:c.2326G>A
ENSP00000463714.1:p.Gly776Ser
ENST00000541774.2:c.2281G>A
ENSP00000446466.1:p.Gly761Ser
ENST00000445658.3:c.1498G>A
ENSP00000404047.2:p.Gly500Ser
ENST00000269571.6:c.2326G>A
ENSP00000269571.4:p.Gly776Ser
ENST00000406381.3:c.2236G>A
ENSP00000385185.2:p.Gly746Ser
ENST00000578373.2:c.*2116G>A
ENST00000584601.2:c.2236G>A
ENSP00000462438.1:p.Gly746Ser

Variation displays