Colon Cancer: Gene >> PIWIL4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000299001
Start	94577389:94577389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.410G>T
AA Mutation	p.Arg137Ile(p.R137I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000299001
Start	94583545:94583545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.611A>G
AA Mutation	p.Gln204Arg(p.Q204R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000299001
Start	94587084:94587084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.751T>C
AA Mutation	p.Ser251Pro(p.S251P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000299001
Start	94583535:94583535(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs554791169
CDS Mutation	c.601G>A
AA Mutation	p.Val201Met(p.V201M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000299001
Start	94619771:94619771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777500348
CDS Mutation	c.2180C>T
AA Mutation	p.Ser727Leu(p.S727L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000299001
Start	94620143:94620143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200034919
CDS Mutation	c.2441C>T
AA Mutation	p.Pro814Leu(p.P814L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000299001
Start	94597872:94597872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1337G>T
AA Mutation	p.Gly446Val(p.G446V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000299001
Start	94607610:94607610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371297833
CDS Mutation	c.1810G>A
AA Mutation	p.Gly604Arg(p.G604R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299001
Start	94607615:94607615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1815C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299001
Start	94577297:94577297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.318G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299001
Start	94595352:94595352(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1194T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000299001
Start	94620021:94620021(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2320delG
AA Mutation	p.Val774TrpfsTer21(p.V774Wfs*21)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PIWIL4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000299001
Start	94583497:94583497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.563C>G
AA Mutation	p.Thr188Ser(p.T188S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000299001
Start	94618029:94618029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2090A>G
AA Mutation	p.Asp697Gly(p.D697G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000299001
Start	94597859:94597859(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750835307
CDS Mutation	c.1324A>G
AA Mutation	p.Ile442Val(p.I442V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000299001
Start	94620951:94620951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2518G>T
AA Mutation	p.Glu840Ter(p.E840*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript