Colon Cancer: Gene >> RLBP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000268125
Start	89217306:89217306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.160G>A
AA Mutation	p.Glu54Lys(p.E54K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000268125
Start	89217245:89217245(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.221C>T
AA Mutation	p.Ala74Val(p.A74V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000268125
Start	89210313:89210313(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.926A>G
AA Mutation	p.Gln309Arg(p.Q309R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000268125
Start	89217251:89217251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772539351
CDS Mutation	c.215C>T
AA Mutation	p.Ala72Val(p.A72V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000268125
Start	89218680:89218680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201258558
CDS Mutation	c.26G>A
AA Mutation	p.Arg9His(p.R9H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268125
Start	89218661:89218661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.45A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268125
Start	89217223:89217223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.243G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268125
Start	89217211:89217211(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs557154377
CDS Mutation	c.255G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000268125
Start	89215077:89215077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.508G>T
AA Mutation	p.Glu170Ter(p.E170*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> RLBP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000268125
Start	89210398:89210398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749162238
CDS Mutation	c.841G>A
AA Mutation	p.Asp281Asn(p.D281N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000268125
Start	89215229:89215229(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.356A>C
AA Mutation	p.Asn119Thr(p.N119T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268125
Start	89215114:89215114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.471G>T
Mutation Classification	Silent
Feature Type	Transcript