Colon Cancer: Gene >> NCAN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000252575
Start	19219055:19219055(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.214G>T
AA Mutation	p.Asp72Tyr(p.D72Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000252575
Start	19224347:19224347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs564199075
CDS Mutation	c.692G>A
AA Mutation	p.Arg231His(p.R231H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000252575
Start	19226608:19226608(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771787600
CDS Mutation	c.1195G>A
AA Mutation	p.Val399Met(p.V399M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000252575
Start	19228081:19228081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2461G>A
AA Mutation	p.Asp821Asn(p.D821N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000252575
Start	19245320:19245320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3500A>C
AA Mutation	p.Glu1167Ala(p.E1167A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000252575
Start	19224066:19224066(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.521C>A
AA Mutation	p.Thr174Asn(p.T174N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000252575
Start	19216982:19216982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.29G>T
AA Mutation	p.Gly10Val(p.G10V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000252575
Start	19219098:19219098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752937778
CDS Mutation	c.257G>A
AA Mutation	p.Gly86Asp(p.G86D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000252575
Start	19227556:19227556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1936C>G
AA Mutation	p.His646Asp(p.H646D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000252575
Start	19218941:19218941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.100G>A
AA Mutation	p.Glu34Lys(p.E34K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000252575
Start	19226579:19226579(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1166A>T
AA Mutation	p.Glu389Val(p.E389V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000252575
Start	19227923:19227923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2303C>T
AA Mutation	p.Thr768Ile(p.T768I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000252575
Start	19245351:19245351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3531C>A
AA Mutation	p.Phe1177Leu(p.F1177L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000252575
Start	19226763:19226763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1350G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000252575
Start	19228560:19228560(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2940A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000252575
Start	19249875:19249875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3930G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000252575
Start	19226917:19226917(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1509delG
AA Mutation	p.Met504TrpfsTer14(p.M504Wfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000252575
Start	19224429:19224429(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.778+1delG
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> NCAN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000252575
Start	19238273:19238273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755391461
CDS Mutation	c.3271G>A
AA Mutation	p.Gly1091Ser(p.G1091S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript