Colon Cancer: Gene >> GIT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000225394
Start	29576988:29576988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767726313
CDS Mutation	c.1102G>A
AA Mutation	p.Glu368Lys(p.E368K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000225394
Start	29578343:29578343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.839C>T
AA Mutation	p.Ala280Val(p.A280V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000225394
Start	29578361:29578361(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374787973
CDS Mutation	c.821G>A
AA Mutation	p.Arg274Gln(p.R274Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000225394
Start	29575849:29575849(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763846891
CDS Mutation	c.1715C>T
AA Mutation	p.Pro572Leu(p.P572L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000225394
Start	29575819:29575819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750445419
CDS Mutation	c.1745G>A
AA Mutation	p.Arg582His(p.R582H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000225394
Start	29574878:29574878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2110C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000225394
Start	29575314:29575314(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1983G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000225394
Start	29576102:29576102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369202718
CDS Mutation	c.1641G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000225394
Start	29576256:29576256(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756882242
CDS Mutation	c.1575C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000225394
Start	29575437:29575438(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1859_1860delAA
AA Mutation	p.Lys620ArgfsTer49(p.K620Rfs*49)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> GIT1

No Mutation Annotation!