Colon Cancer: Gene >> PHF10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000339209
Start	169715989:169715989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747615034
CDS Mutation	c.509G>A
AA Mutation	p.Arg170His(p.R170H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000339209
Start	169721009:169721009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.190C>A
AA Mutation	p.Leu64Ile(p.L64I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000339209
Start	169716073:169716073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770677813
CDS Mutation	c.425G>A
AA Mutation	p.Arg142His(p.R142H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000339209
Start	169715959:169715959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.539A>T
AA Mutation	p.Tyr180Phe(p.Y180F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000339209
Start	169721040:169721040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.159T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000339209
Start	169705644:169705644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1194T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000339209
Start	169717860:169717860(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.372A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000339209
Start	169715783:169715783(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.618delA
AA Mutation	p.Ala207GlnfsTer8(p.A207Qfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000339209
Start	169704052:169704052(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1448delC
AA Mutation	p.Pro483GlnfsTer?(p.P483Qfs*?)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000339209
Start	169718786:169718786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.325+2T>G
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> PHF10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000339209
Start	169715846:169715846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.555A>T
AA Mutation	p.Gln185His(p.Q185H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000339209
Start	169705303:169705303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1241A>G
AA Mutation	p.Asp414Gly(p.D414G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000339209
Start	169710288:169710288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1061G>T
AA Mutation	p.Arg354Ile(p.R354I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript