Colon Cancer: Gene >> CRIM1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000280527
Start	36441285:36441285(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138252009
CDS Mutation	c.533G>A
AA Mutation	p.Arg178His(p.R178H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000280527
Start	36442665:36442665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs560635455
CDS Mutation	c.799G>A
AA Mutation	p.Ala267Thr(p.A267T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000280527
Start	36479572:36479572(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767565422
CDS Mutation	c.1250G>A
AA Mutation	p.Arg417Gln(p.R417Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000280527
Start	36513679:36513679(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1904G>A
AA Mutation	p.Arg635Gln(p.R635Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000280527
Start	36476970:36476970(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761241012
CDS Mutation	c.1073G>A
AA Mutation	p.Arg358Gln(p.R358Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000280527
Start	36356326:36356326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.34G>A
AA Mutation	p.Gly12Ser(p.G12S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000280527
Start	36548526:36548526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2936C>A
AA Mutation	p.Pro979His(p.P979H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000280527
Start	36441490:36441490(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.738G>T
AA Mutation	p.Glu246Asp(p.E246D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000280527
Start	36544461:36544461(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2709C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000280527
Start	36544455:36544455(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2703G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000280527
Start	36479543:36479543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1221C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000280527
Start	36479621:36479621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1299C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000280527
Start	36476905:36476905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766022040
CDS Mutation	c.1008C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000280527
Start	36396690:36396690(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.408C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000280527
Start	36464537:36464537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748318484
CDS Mutation	c.873C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000280527
Start	36537485:36537485(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2567delC
AA Mutation	p.Pro856LeufsTer67(p.P856Lfs*67)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000280527
Start	36442613:36442613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.749-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> CRIM1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000280527
Start	36396644:36396644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.362G>A
AA Mutation	p.Gly121Asp(p.G121D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000280527
Start	36544450:36544450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2698C>T
AA Mutation	p.Pro900Ser(p.P900S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000280527
Start	36522240:36522240(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2355C>A
AA Mutation	p.Phe785Leu(p.F785L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000280527
Start	36547138:36547138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2901A>G
AA Mutation	p.Ile967Met(p.I967M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000280527
Start	36548553:36548553(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2963C>T
AA Mutation	p.Ser988Phe(p.S988F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000280527
Start	36513647:36513647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764953903
CDS Mutation	c.1872T>C
Mutation Classification	Silent
Feature Type	Transcript