Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> NIT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368009
Start	161120578:161120578(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.797G>T
AA Mutation	p.Arg266Ile(p.R266I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000368009
Start	161119902:161119902(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs531981250
CDS Mutation	c.541A>G
AA Mutation	p.Thr181Ala(p.T181A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000368009
Start	161119570:161119570(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759711881
CDS Mutation	c.415A>G
AA Mutation	p.Thr139Ala(p.T139A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368009
Start	161119149:161119149(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758069016
CDS Mutation	c.114T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368009
Start	161120187:161120187(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.672C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	start_lost;splice_region_variant
Transcription ID	ENST00000368009
Start	161118786:161118786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3G>A
AA Mutation	p.Met1?(p.M1?)
Mutation Classification	Translation_Start_Site
Feature Type	Transcript

Rectum Cancer: Gene >> NIT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368009
Start	161119849:161119849(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.488A>T
AA Mutation	p.His163Leu(p.H163L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368009
Start	161119847:161119847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.486A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368009
Start	161118819:161118819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.36C>T
Mutation Classification	Silent
Feature Type	Transcript