Colon Cancer: Gene >> NHEJ1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356853
Start	219078105:219078105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.690G>T
AA Mutation	p.Gln230His(p.Q230H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356853
Start	219078167:219078167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.628T>G
AA Mutation	p.Phe210Val(p.F210V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000356853
Start	219147668:219147668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770861190
CDS Mutation	c.518C>T
AA Mutation	p.Thr173Met(p.T173M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356853
Start	219147720:219147720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.466T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356853
Start	219147676:219147676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.510T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> NHEJ1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356853
Start	219146735:219146735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.533G>A
AA Mutation	p.Arg178Gln(p.R178Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000356853
Start	219147660:219147660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.526C>T
AA Mutation	p.Arg176Ter(p.R176*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript