Colon Cancer: Gene >> RAD51C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000337432
Start	58734136:58734136(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1045A>G
AA Mutation	p.Thr349Ala(p.T349A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000337432
Start	58696755:58696755(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.467T>C
AA Mutation	p.Val156Ala(p.V156A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000337432
Start	58724069:58724069(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs730881932
CDS Mutation	c.934C>T
AA Mutation	p.Arg312Trp(p.R312W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000337432
Start	58692670:58692670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.27A>C
AA Mutation	p.Glu9Asp(p.E9D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000337432
Start	58709946:58709946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.793C>A
AA Mutation	p.Leu265Ile(p.L265I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000337432
Start	58696699:58696699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.411G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000337432
Start	58695099:58695099(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.314delC
AA Mutation	p.Ser105Ter(p.S105*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> RAD51C

No Mutation Annotation!