Colon Cancer: Gene >> SIAE

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263593
Start	124638566:124638566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1296G>T
AA Mutation	p.Gln432His(p.Q432H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263593
Start	124660747:124660747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375087861
CDS Mutation	c.286G>A
AA Mutation	p.Glu96Lys(p.E96K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263593
Start	124637156:124637156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201702369
CDS Mutation	c.1367T>C
AA Mutation	p.Met456Thr(p.M456T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000263593
Start	124637105:124637105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1418G>A
AA Mutation	p.Gly473Asp(p.G473D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000263593
Start	124638588:124638588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774599983
CDS Mutation	c.1274A>G
AA Mutation	p.Tyr425Cys(p.Y425C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000263593
Start	124649793:124649793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.548A>C
AA Mutation	p.Asn183Thr(p.N183T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000263593
Start	124669472:124669472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.117G>T
AA Mutation	p.Gln39His(p.Q39H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SIAE

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263593
Start	124636967:124636967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1556G>A
AA Mutation	p.Ser519Asn(p.S519N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263593
Start	124669413:124669413(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.176T>C
AA Mutation	p.Val59Ala(p.V59A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000263593
Start	124638625:124638625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1237G>T
AA Mutation	p.Glu413Ter(p.E413*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript