Colon Cancer: Gene >> NACC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000292431
Start	13135341:13135341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.134G>A
AA Mutation	p.Arg45Gln(p.R45Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000292431
Start	13138221:13138221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1399G>A
AA Mutation	p.Ala467Thr(p.A467T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000292431
Start	13137375:13137375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1225C>T
AA Mutation	p.Arg409Trp(p.R409W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000292431
Start	13137527:13137527(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1276G>A
AA Mutation	p.Asp426Asn(p.D426N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000292431
Start	13138245:13138245(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1423T>G
AA Mutation	p.Trp475Gly(p.W475G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000292431
Start	13135278:13135278(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.71G>A
AA Mutation	p.Arg24Gln(p.R24Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000292431
Start	13135472:13135472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368391948
CDS Mutation	c.265C>T
AA Mutation	p.Arg89Trp(p.R89W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000292431
Start	13136342:13136342(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1057A>C
AA Mutation	p.Asn353His(p.N353H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000292431
Start	13135645:13135645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764392858
CDS Mutation	c.438C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000292431
Start	13135492:13135492(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143634134
CDS Mutation	c.285C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> NACC1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000292431
Start	13135516:13135516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138480405
CDS Mutation	c.309G>A
Mutation Classification	Silent
Feature Type	Transcript