Colon Cancer: Gene >> HECA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367658
Start	139166639:139166639(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.627G>T
AA Mutation	p.Lys209Asn(p.K209N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367658
Start	139167136:139167136(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1124G>A
AA Mutation	p.Gly375Asp(p.G375D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367658
Start	139166477:139166477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.465C>G
AA Mutation	p.Asn155Lys(p.N155K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000367658
Start	139174520:139174520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1448C>T
AA Mutation	p.Ala483Val(p.A483V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000367658
Start	139174448:139174448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1376G>A
AA Mutation	p.Cys459Tyr(p.C459Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000367658
Start	139167108:139167108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759180001
CDS Mutation	c.1096G>A
AA Mutation	p.Val366Met(p.V366M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000367658
Start	139166460:139166460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760164332
CDS Mutation	c.448C>T
AA Mutation	p.Arg150Cys(p.R150C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367658
Start	139166459:139166459(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.447C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367658
Start	139167047:139167047(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1035G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367658
Start	139177063:139177063(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767636851
CDS Mutation	c.1590C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367658
Start	139166627:139166627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776074028
CDS Mutation	c.615T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367658
Start	139167010:139167010(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1004delG
AA Mutation	p.Gly335AspfsTer27(p.G335Dfs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367658
Start	139166460:139166461(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.455_456delGC
AA Mutation	p.Arg152GlnfsTer65(p.R152Qfs*65)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367658
Start	139166677:139166678(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.671dupA
AA Mutation	p.Cys225ValfsTer6(p.C225Vfs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> HECA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367658
Start	139167000:139167000(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.988G>T
AA Mutation	p.Ala330Ser(p.A330S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367658
Start	139176980:139176980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1507G>A
AA Mutation	p.Asp503Asn(p.D503N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript