Colon Cancer: Gene >> RBBP8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000327155
Start	23026187:23026187(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760773711
CDS Mutation	c.2641C>T
AA Mutation	p.Arg881Cys(p.R881C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000327155
Start	22982346:22982346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.557A>G
AA Mutation	p.Tyr186Cys(p.Y186C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000327155
Start	22993532:22993532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1705C>A
AA Mutation	p.Pro569Thr(p.P569T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000327155
Start	23026225:23026225(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2679G>T
AA Mutation	p.Lys893Asn(p.K893N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000327155
Start	22968829:22968829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369500650
CDS Mutation	c.272G>A
AA Mutation	p.Arg91His(p.R91H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000327155
Start	23026158:23026158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2612A>G
AA Mutation	p.Asp871Gly(p.D871G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000327155
Start	22989310:22989310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.799G>A
AA Mutation	p.Glu267Lys(p.E267K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327155
Start	23026225:23026225(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2679G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000327155
Start	22975185:22975185(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.398delA
AA Mutation	p.Lys133SerfsTer33(p.K133Sfs*33)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> RBBP8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000327155
Start	22993061:22993061(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1234A>G
AA Mutation	p.Ile412Val(p.I412V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000327155
Start	22949637:22949637(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.172G>A
AA Mutation	p.Glu58Lys(p.E58K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000327155
Start	22993038:22993038(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1211A>C
AA Mutation	p.Lys404Thr(p.K404T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript