Colon Cancer: Gene >> NCKIPSD

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000294129
Start	48679392:48679392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1555C>T
AA Mutation	p.Pro519Ser(p.P519S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000294129
Start	48682970:48682970(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.214G>A
AA Mutation	p.Glu72Lys(p.E72K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000294129
Start	48674603:48674603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762789060
CDS Mutation	c.2110C>T
AA Mutation	p.Arg704Cys(p.R704C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000294129
Start	48679171:48679171(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775376697
CDS Mutation	c.1583C>T
AA Mutation	p.Thr528Met(p.T528M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000294129
Start	48679163:48679163(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779589441
CDS Mutation	c.1591G>A
AA Mutation	p.Ala531Thr(p.A531T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294129
Start	48682097:48682097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771858876
CDS Mutation	c.546G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294129
Start	48680089:48680089(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1233C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294129
Start	48678597:48678597(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1932G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> NCKIPSD

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000294129
Start	48681708:48681708(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.671A>G
AA Mutation	p.Asp224Gly(p.D224G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript