Colon Cancer: Gene >> ITPKC

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263370
Start	40729360:40729360(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1414G>T
AA Mutation	p.Asp472Tyr(p.D472Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263370
Start	40733243:40733243(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1553A>G
AA Mutation	p.Asp518Gly(p.D518G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263370
Start	40718021:40718021(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.886G>A
AA Mutation	p.Gly296Arg(p.G296R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000263370
Start	40725418:40725418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1234G>A
AA Mutation	p.Val412Ile(p.V412I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000263370
Start	40733209:40733209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1519C>T
AA Mutation	p.Arg507Trp(p.R507W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000263370
Start	40717836:40717836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.701A>G
AA Mutation	p.Gln234Arg(p.Q234R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000263370
Start	40733297:40733297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1607G>A
AA Mutation	p.Arg536His(p.R536H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000263370
Start	40733308:40733308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1618T>C
AA Mutation	p.Trp540Arg(p.W540R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000263370
Start	40739427:40739427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1919G>A
AA Mutation	p.Gly640Asp(p.G640D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263370
Start	40717681:40717681(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.546G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263370
Start	40717915:40717915(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.780A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000263370
Start	40718292:40718292(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1155+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> ITPKC

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263370
Start	40739384:40739384(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1876C>G
AA Mutation	p.His626Asp(p.H626D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript