Colon Cancer: Gene >> PRDM14

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000276594
Start	70052280:70052280(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148573764
CDS Mutation	c.1513C>T
AA Mutation	p.Arg505Cys(p.R505C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000276594
Start	70069457:70069457(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.404G>A
AA Mutation	p.Gly135Asp(p.G135D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000276594
Start	70069640:70069640(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.221C>T
AA Mutation	p.Ala74Val(p.A74V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000276594
Start	70052195:70052195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1598A>T
AA Mutation	p.Asp533Val(p.D533V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000276594
Start	70069497:70069497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.364G>A
AA Mutation	p.Ala122Thr(p.A122T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000276594
Start	70052279:70052279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762086448
CDS Mutation	c.1514G>A
AA Mutation	p.Arg505His(p.R505H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000276594
Start	70058752:70058752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1274T>C
AA Mutation	p.Val425Ala(p.V425A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000276594
Start	70066382:70066382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1036G>T
AA Mutation	p.Gly346Trp(p.G346W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000276594
Start	70069212:70069212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.649G>A
AA Mutation	p.Ala217Thr(p.A217T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000276594
Start	70069701:70069701(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.160C>T
AA Mutation	p.Arg54Trp(p.R54W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000276594
Start	70069585:70069585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766237068
CDS Mutation	c.276G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000276594
Start	70069777:70069777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.84G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000276594
Start	70069318:70069318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.543T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000276594
Start	70069834:70069834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.27C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000276594
Start	70069558:70069558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.303G>A
AA Mutation	p.Trp101Ter(p.W101*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> PRDM14

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000276594
Start	70058684:70058684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1342C>T
AA Mutation	p.Arg448Trp(p.R448W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000276594
Start	70058793:70058793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1233C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000276594
Start	70069807:70069807(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.54G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000276594
Start	70052143:70052143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1650C>A
Mutation Classification	Silent
Feature Type	Transcript