Colon Cancer: Gene >> NOD1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000222823
Start	30452392:30452392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1025T>C
AA Mutation	p.Phe342Ser(p.F342S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000222823
Start	30452056:30452056(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1361A>T
AA Mutation	p.His454Leu(p.H454L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000222823
Start	30451765:30451765(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs570225517
CDS Mutation	c.1652C>T
AA Mutation	p.Ala551Val(p.A551V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000222823
Start	30451358:30451358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201927568
CDS Mutation	c.2059G>A
AA Mutation	p.Ala687Thr(p.A687T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000222823
Start	30446988:30446988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773339280
CDS Mutation	c.2348G>A
AA Mutation	p.Cys783Tyr(p.C783Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000222823
Start	30455237:30455237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.276A>C
AA Mutation	p.Gln92His(p.Q92H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000222823
Start	30451940:30451940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1477A>G
AA Mutation	p.Met493Val(p.M493V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000222823
Start	30447002:30447002(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2334A>C
AA Mutation	p.Lys778Asn(p.K778N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000222823
Start	30452727:30452727(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.690C>A
AA Mutation	p.Phe230Leu(p.F230L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222823
Start	30446975:30446975(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs189173990
CDS Mutation	c.2361G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222823
Start	30452343:30452343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754556858
CDS Mutation	c.1074C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222823
Start	30452358:30452358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1059C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000222823
Start	30451768:30451768(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1649delC
AA Mutation	p.Pro550LeufsTer64(p.P550Lfs*64)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> NOD1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000222823
Start	30452714:30452714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.703C>T
AA Mutation	p.Arg235Cys(p.R235C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000222823
Start	30437628:30437630(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2480_2482delAAG
AA Mutation	p.Glu827del(p.E827del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript