Colon Cancer: Gene >> IFRD2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000417626
Start	50290638:50290638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782102310
CDS Mutation	c.292G>A
AA Mutation	p.Asp98Asn(p.D98N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000417626
Start	50288419:50288419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1430G>A
AA Mutation	p.Arg477His(p.R477H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000417626
Start	50290457:50290457(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.386A>G
AA Mutation	p.Asp129Gly(p.D129G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000417626
Start	50290036:50290036(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782709559
CDS Mutation	c.631G>A
AA Mutation	p.Val211Met(p.V211M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000417626
Start	50288228:50288228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369995042
CDS Mutation	c.1484G>A
AA Mutation	p.Arg495Gln(p.R495Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000417626
Start	50290170:50290170(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.580G>T
AA Mutation	p.Gly194Trp(p.G194W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000417626
Start	50288488:50288488(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782161246
CDS Mutation	c.1361G>A
AA Mutation	p.Arg454His(p.R454H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000417626
Start	50289310:50289310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201634662
CDS Mutation	c.1022G>A
AA Mutation	p.Arg341Gln(p.R341Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000417626
Start	50290642:50290642(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.288T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000417626
Start	50289567:50289567(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.851delG
AA Mutation	p.Gly284AlafsTer55(p.G284Afs*55)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> IFRD2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000417626
Start	50288891:50288891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1124G>A
AA Mutation	p.Arg375His(p.R375H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript