Colon Cancer: Gene >> RALGDS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372050
Start	133108184:133108184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1001A>G
AA Mutation	p.Glu334Gly(p.E334G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000372050
Start	133100270:133100270(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779876054
CDS Mutation	c.2567G>A
AA Mutation	p.Arg856Gln(p.R856Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000372050
Start	133109705:133109705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.505G>A
AA Mutation	p.Ala169Thr(p.A169T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000372050
Start	133101954:133101954(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2195A>G
AA Mutation	p.Asp732Gly(p.D732G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000372050
Start	133098631:133098631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2701C>T
AA Mutation	p.Arg901Cys(p.R901C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000372050
Start	133103781:133103781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1724T>C
AA Mutation	p.Val575Ala(p.V575A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000372050
Start	133108343:133108343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745523786
CDS Mutation	c.842G>A
AA Mutation	p.Arg281Gln(p.R281Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000372050
Start	133098744:133098744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2588A>G
AA Mutation	p.Asn863Ser(p.N863S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000372050
Start	133101656:133101656(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs561121466
CDS Mutation	c.2318G>A
AA Mutation	p.Arg773His(p.R773H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000372050
Start	133106675:133106675(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs550664081
CDS Mutation	c.1487G>A
AA Mutation	p.Arg496His(p.R496H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372050
Start	133102097:133102097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2052C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372050
Start	133107208:133107208(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1290C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372050
Start	133108857:133108857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.594C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372050
Start	133102838:133102838(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143850838
CDS Mutation	c.1854G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372050
Start	133100290:133100290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2547G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000372050
Start	133109626:133109626(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.584delA
AA Mutation	p.Asn195MetfsTer73(p.N195Mfs*73)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> RALGDS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372050
Start	133108059:133108059(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1126A>C
AA Mutation	p.Ser376Arg(p.S376R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372050
Start	133108291:133108291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.894A>C
Mutation Classification	Silent
Feature Type	Transcript