Colon Cancer: Gene >> CHN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000409900
Start	174877986:174877986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.403G>A
AA Mutation	p.Ala135Thr(p.A135T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000409900
Start	174944910:174944910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.92G>A
AA Mutation	p.Arg31Gln(p.R31Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000409900
Start	174812375:174812375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373546784
CDS Mutation	c.820G>A
AA Mutation	p.Val274Met(p.V274M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000409900
Start	174877841:174877841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.548G>A
AA Mutation	p.Arg183Lys(p.R183K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000409900
Start	174824512:174824512(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.634A>G
AA Mutation	p.Thr212Ala(p.T212A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000409900
Start	174878091:174878091(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.298G>A
AA Mutation	p.Asp100Asn(p.D100N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000409900
Start	174915140:174915140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs557351535
CDS Mutation	c.178G>A
AA Mutation	p.Asp60Asn(p.D60N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000409900
Start	174878103:174878103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.286A>T
AA Mutation	p.Arg96Trp(p.R96W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000409900
Start	174846889:174846889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.618C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000409900
Start	174877846:174877846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.543G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000409900
Start	174800275:174800275(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765073937
CDS Mutation	c.1221C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000409900
Start	174944900:174944900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.102C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000409900
Start	174878104:174878105(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.284_285insGTATG
AA Mutation	p.Phe95LeufsTer25(p.F95Lfs*25)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CHN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000409900
Start	174846937:174846937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.570A>T
AA Mutation	p.Arg190Ser(p.R190S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000409900
Start	174801714:174801714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1201C>A
AA Mutation	p.Leu401Ile(p.L401I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript