Colon Cancer: Gene >> NBL1

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000375136
Start	19655326:19655326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778071969
CDS Mutation	c.173C>T
AA Mutation	p.Ala58Val(p.A58V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000375136
Start	19655374:19655374(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.221A>C
AA Mutation	p.Gln74Pro(p.Q74P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000375136
Start	19656882:19656882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750974701
CDS Mutation	c.299C>T
AA Mutation	p.Pro100Leu(p.P100L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375136
Start	19656970:19656970(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776840933
CDS Mutation	c.387C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000375136
Start	19657095:19657095(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.517delC
AA Mutation	p.His173ThrfsTer37(p.H173Tfs*37)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> NBL1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375136
Start	19656991:19656991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.408G>T
Mutation Classification	Silent
Feature Type	Transcript