Colon Cancer: Gene >> PARVB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000338758
Start	44131540:44131540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.430G>T
AA Mutation	p.Gly144Trp(p.G144W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000338758
Start	44163876:44163876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749414411
CDS Mutation	c.964G>A
AA Mutation	p.Ala322Thr(p.A322T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000338758
Start	44133007:44133007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750285011
CDS Mutation	c.631C>T
AA Mutation	p.Arg211Trp(p.R211W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000338758
Start	44158033:44158033(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.895T>G
AA Mutation	p.Phe299Val(p.F299V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000338758
Start	44119052:44119052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.288G>T
AA Mutation	p.Trp96Cys(p.W96C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000338758
Start	44163925:44163925(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1013C>T
AA Mutation	p.Pro338Leu(p.P338L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000338758
Start	44136478:44136478(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.652C>A
AA Mutation	p.His218Asn(p.H218N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000338758
Start	44100067:44100067(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370343316
CDS Mutation	c.217C>T
AA Mutation	p.Arg73Cys(p.R73C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338758
Start	44147910:44147910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772503278
CDS Mutation	c.762C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338758
Start	44147881:44147881(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.733C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000338758
Start	44147868:44147868(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.720delT
AA Mutation	p.Asp240GlufsTer17(p.D240Efs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PARVB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000338758
Start	44157992:44157992(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.854G>A
AA Mutation	p.Gly285Asp(p.G285D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000338758
Start	44131507:44131507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.397C>A
AA Mutation	p.Leu133Met(p.L133M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338758
Start	44093980:44093980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369214399
CDS Mutation	c.165C>T
Mutation Classification	Silent
Feature Type	Transcript