Colon Cancer: Gene >> ITCH

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262650
Start	34479699:34479699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778741830
CDS Mutation	c.1851G>T
AA Mutation	p.Lys617Asn(p.K617N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262650
Start	34412547:34412547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767950508
CDS Mutation	c.245G>A
AA Mutation	p.Arg82His(p.R82H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262650
Start	34507703:34507703(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2621G>A
AA Mutation	p.Arg874His(p.R874H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000262650
Start	34412639:34412639(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199947085
CDS Mutation	c.337C>T
AA Mutation	p.Leu113Phe(p.L113F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262650
Start	34438587:34438587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs540203213
CDS Mutation	c.758C>T
AA Mutation	p.Pro253Leu(p.P253L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000262650
Start	34477814:34477814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1735G>A
AA Mutation	p.Val579Met(p.V579M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000262650
Start	34481100:34481100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2110T>C
AA Mutation	p.Tyr704His(p.Y704H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000262650
Start	34462202:34462202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1528C>A
AA Mutation	p.Arg510Ser(p.R510S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262650
Start	34408739:34408739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.159G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262650
Start	34445386:34445386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1188C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262650
Start	34471485:34471485(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1666delA
AA Mutation	p.Thr556HisfsTer10(p.T556Hfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ITCH

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262650
Start	34492535:34492535(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2477G>A
AA Mutation	p.Arg826Lys(p.R826K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262650
Start	34424520:34424520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.639A>C
AA Mutation	p.Glu213Asp(p.E213D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript