DoCM - Database of Curated Mutations

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Variant Data

Location

HGVS: ENST00000374632:c.2359G>A
Reference Version: GRCh37
Chromosome: 1
Start: 23235518
Stop: 23235518
Strand: 1
Transcript: ENST00000374632 (ensembl - 74_37)
Gene: EPHB2 ( View drug interactions on DGIdb )

Information

Reference: G
Variant: A
Amino Acid: p.G787R
Mutation Type: missense
Variant Type: SNV (SO:0001483)
cDNA Change: c.2359
Tags: inactivating likely pathogenic

Disease Data

Disease	Source	Batch	Tags	External Links
colorectal cancer	Zogopoulos et al., 2008, PLoS ONE	Kin-Driver (View variants)	inactivating likely pathogenic

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