Colon Cancer: Gene >> RAD51D

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000345365
Start	35118600:35118600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs151198586
CDS Mutation	c.164G>A
AA Mutation	p.Arg55Gln(p.R55Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000345365
Start	35106441:35106441(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.521A>T
AA Mutation	p.Asp174Val(p.D174V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000345365
Start	35107064:35107064(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.404T>C
AA Mutation	p.Val135Ala(p.V135A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345365
Start	35118506:35118506(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.258T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345365
Start	35101001:35101001(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.939C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000345365
Start	35103268:35103269(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.723dupT
AA Mutation	p.Gly242TrpfsTer85(p.G242Wfs*85)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> RAD51D

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000345365
Start	35107439:35107439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.272A>C
AA Mutation	p.Lys91Thr(p.K91T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000345365
Start	35101346:35101346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.758G>A
AA Mutation	p.Arg253Gln(p.R253Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript