Colon Cancer: Gene >> ICAM5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000221980
Start	10293779:10293779(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1547C>T
AA Mutation	p.Ala516Val(p.A516V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000221980
Start	10292708:10292708(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1058C>T
AA Mutation	p.Thr353Ile(p.T353I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000221980
Start	10295424:10295424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2309G>A
AA Mutation	p.Arg770His(p.R770H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000221980
Start	10293835:10293835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765026177
CDS Mutation	c.1603G>A
AA Mutation	p.Val535Ile(p.V535I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000221980
Start	10293889:10293889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1657G>A
AA Mutation	p.Glu553Lys(p.E553K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000221980
Start	10292062:10292062(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139899408
CDS Mutation	c.701C>T
AA Mutation	p.Ala234Val(p.A234V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000221980
Start	10291321:10291321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.332G>A
AA Mutation	p.Arg111His(p.R111H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000221980
Start	10293853:10293853(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1621C>T
AA Mutation	p.Arg541Cys(p.R541C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000221980
Start	10291783:10291783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.647C>T
AA Mutation	p.Ser216Leu(p.S216L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000221980
Start	10294062:10294062(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1734G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000221980
Start	10293026:10293026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1245C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000221980
Start	10294600:10294600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2190G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000221980
Start	10292279:10292279(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.923delG
AA Mutation	p.Gly308AlafsTer10(p.G308Afs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000221980
Start	10295378:10295378(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2267delC
AA Mutation	p.Pro756LeufsTer12(p.P756Lfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000221980
Start	10292256:10292256(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.895C>T
AA Mutation	p.Gln299Ter(p.Q299*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ICAM5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000221980
Start	10295370:10295370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2255C>T
AA Mutation	p.Ala752Val(p.A752V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000221980
Start	10292848:10292848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1198G>A
AA Mutation	p.Ala400Thr(p.A400T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000221980
Start	10294088:10294088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1760T>C
AA Mutation	p.Val587Ala(p.V587A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000221980
Start	10292159:10292159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.798G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000221980
Start	10292279:10292279(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.923delG
AA Mutation	p.Gly308AlafsTer10(p.G308Afs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000221980
Start	10293823:10293823(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1591G>T
AA Mutation	p.Glu531Ter(p.E531*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript