Colon Cancer: Gene >> CHAT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000337653
Start	49619831:49619831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.494T>G
AA Mutation	p.Ile165Ser(p.I165S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000337653
Start	49662779:49662779(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1974C>A
AA Mutation	p.Ser658Arg(p.S658R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000337653
Start	49646567:49646567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs115877658
CDS Mutation	c.1174G>A
AA Mutation	p.Ala392Thr(p.A392T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000337653
Start	49614314:49614314(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.125G>A
AA Mutation	p.Arg42His(p.R42H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000337653
Start	49664862:49664862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2063C>A
AA Mutation	p.Thr688Asn(p.T688N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000337653
Start	49655422:49655422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1813C>T
AA Mutation	p.Arg605Cys(p.R605C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000337653
Start	49662760:49662760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs116628504
CDS Mutation	c.1955G>A
AA Mutation	p.Arg652Gln(p.R652Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000337653
Start	49646642:49646642(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1249G>A
AA Mutation	p.Gly417Arg(p.G417R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000337653
Start	49646646:49646646(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376230019
CDS Mutation	c.1253C>T
AA Mutation	p.Ala418Val(p.A418V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000337653
Start	49627639:49627639(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.965G>A
AA Mutation	p.Arg322His(p.R322H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000337653
Start	49655129:49655129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372760913
CDS Mutation	c.1669G>A
AA Mutation	p.Ala557Thr(p.A557T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000337653
Start	49614236:49614236(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.47A>C
AA Mutation	p.Lys16Thr(p.K16T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000337653
Start	49649545:49649545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371719364
CDS Mutation	c.1420G>A
AA Mutation	p.Val474Ile(p.V474I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000337653
Start	49655130:49655130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769204680
CDS Mutation	c.1670C>T
AA Mutation	p.Ala557Val(p.A557V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000337653
Start	49649566:49649566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751583653
CDS Mutation	c.1441C>T
AA Mutation	p.Arg481Trp(p.R481W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000337653
Start	49627610:49627610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.936C>A
AA Mutation	p.Phe312Leu(p.F312L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000337653
Start	49625541:49625541(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.821A>G
AA Mutation	p.Tyr274Cys(p.Y274C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000337653
Start	49648545:49648545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766466820
CDS Mutation	c.1320C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000337653
Start	49616593:49616593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.378T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000337653
Start	49619895:49619895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.558G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000337653
Start	49655128:49655128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs55702495
CDS Mutation	c.1668C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000337653
Start	49619746:49619746(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.413delC
AA Mutation	p.Pro138ArgfsTer62(p.P138Rfs*62)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CHAT

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000337653
Start	49651932:49651932(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1560G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000337653
Start	49664969:49664969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2170C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000337653
Start	49614271:49614271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.82A>C
Mutation Classification	Silent
Feature Type	Transcript