Colon Cancer: Gene >> RALBP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000019317
Start	9517107:9517107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.507G>T
AA Mutation	p.Lys169Asn(p.K169N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000019317
Start	9517161:9517161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.561A>C
AA Mutation	p.Lys187Asn(p.K187N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000019317
Start	9535809:9535809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750108400
CDS Mutation	c.1840C>T
AA Mutation	p.Arg614Cys(p.R614C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000019317
Start	9522369:9522369(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.913C>T
AA Mutation	p.Arg305Cys(p.R305C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000019317
Start	9513200:9513200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.155A>G
AA Mutation	p.Asp52Gly(p.D52G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000019317
Start	9533425:9533425(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1546C>T
AA Mutation	p.Arg516Cys(p.R516C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000019317
Start	9517056:9517056(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.456A>C
AA Mutation	p.Lys152Asn(p.K152N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000019317
Start	9530915:9530915(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1429G>C
AA Mutation	p.Glu477Gln(p.E477Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000019317
Start	9530916:9530916(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1430A>T
AA Mutation	p.Glu477Val(p.E477V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000019317
Start	9535904:9535904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377586790
CDS Mutation	c.1935G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000019317
Start	9535784:9535784(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1815G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000019317
Start	9522381:9522381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.925G>T
AA Mutation	p.Glu309Ter(p.E309*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> RALBP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000019317
Start	9524702:9524702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1162A>C
AA Mutation	p.Met388Leu(p.M388L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000019317
Start	9530920:9530920(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1434T>G
Mutation Classification	Silent
Feature Type	Transcript