Original source

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

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

Chromosome 17:37880997 (forward strand) | View in location tab

Co-located

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

Most severe consequence
Evidence status

Clinical significance

This variation has 4 synonyms - click the plus to show

This variation has 19 HGVS names - click the plus to show

17:g.37880997G>A
ENST00000583038.1:n.3460G>A
ENST00000580074.1:c.432G>A
ENSP00000463002.1:p.Gly145Ser
ENST00000584450.1:c.2326G>A
ENSP00000463714.1:p.Gly776Ser
ENST00000541774.1:c.2281G>A
ENSP00000446466.1:p.Gly761Ser
ENST00000445658.2:c.1498G>A
ENSP00000404047.2:p.Gly500Ser
ENST00000269571.5:c.2326G>A
ENSP00000269571.4:p.Gly776Ser
ENST00000406381.2:c.2236G>A
ENSP00000385185.2:p.Gly746Ser
ENST00000578373.1:c.*2116G>A
ENST00000540147.1:c.2236G>A
ENSP00000443562.1:p.Gly746Ser
ENST00000584601.1:c.2236G>A
ENSP00000462438.1:p.Gly746Ser

Variation displays