Colon Cancer: Gene >> ICAM1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264832
Start	10274969:10274969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.272T>C
AA Mutation	p.Met91Thr(p.M91T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264832
Start	10284813:10284813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs112301533
CDS Mutation	c.1211C>T
AA Mutation	p.Pro404Leu(p.P404L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264832
Start	10284576:10284576(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139178890
CDS Mutation	c.1099C>T
AA Mutation	p.Arg367Cys(p.R367C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000264832
Start	10284573:10284573(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370415118
CDS Mutation	c.1096G>A
AA Mutation	p.Gly366Arg(p.G366R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000264832
Start	10285121:10285121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780437504
CDS Mutation	c.1433G>A
AA Mutation	p.Arg478Gln(p.R478Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000264832
Start	10285156:10285156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775418785
CDS Mutation	c.1468G>A
AA Mutation	p.Ala490Thr(p.A490T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264832
Start	10283686:10283686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.537C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264832
Start	10274943:10274943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.246C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264832
Start	10284985:10284985(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1383C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264832
Start	10284413:10284413(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199692247
CDS Mutation	c.936G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ICAM1

No Mutation Annotation!