Colon Cancer: Gene >> TICAM1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000248244
Start	4818140:4818140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199816697
CDS Mutation	c.238G>A
AA Mutation	p.Val80Met(p.V80M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000248244
Start	4817983:4817983(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755557071
CDS Mutation	c.395G>A
AA Mutation	p.Arg132Gln(p.R132Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000248244
Start	4816730:4816730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146110283
CDS Mutation	c.1648C>T
AA Mutation	p.Arg550Trp(p.R550W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000248244
Start	4817888:4817888(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.490T>C
AA Mutation	p.Cys164Arg(p.C164R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000248244
Start	4817593:4817593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.785C>T
AA Mutation	p.Ala262Val(p.A262V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000248244
Start	4816328:4816328(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376421303
CDS Mutation	c.2050G>A
AA Mutation	p.Ala684Thr(p.A684T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000248244
Start	4817093:4817093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1285G>A
AA Mutation	p.Glu429Lys(p.E429K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000248244
Start	4817069:4817069(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766706840
CDS Mutation	c.1309G>A
AA Mutation	p.Gly437Arg(p.G437R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000248244
Start	4817504:4817504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200901007
CDS Mutation	c.874G>A
AA Mutation	p.Ala292Thr(p.A292T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000248244
Start	4816998:4816998(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1380C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000248244
Start	4816788:4816788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1590C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000248244
Start	4817979:4817979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.399G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000248244
Start	4817382:4817382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199935588
CDS Mutation	c.996G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000248244
Start	4817778:4817778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.600T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000248244
Start	4817682:4817682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs574449966
CDS Mutation	c.696C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000248244
Start	4816453:4816453(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1925delC
AA Mutation	p.Pro642HisfsTer50(p.P642Hfs*50)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000248244
Start	4817957:4817957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs387907307
CDS Mutation	c.421C>T
AA Mutation	p.Arg141Ter(p.R141*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TICAM1

No Mutation Annotation!