Colon Cancer: Gene >> PHF20

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374012
Start	35871785:35871785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369867507
CDS Mutation	c.1238C>T
AA Mutation	p.Pro413Leu(p.P413L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374012
Start	35863366:35863366(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.774A>C
AA Mutation	p.Arg258Ser(p.R258S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000374012
Start	35871105:35871105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs151029211
CDS Mutation	c.1073C>T
AA Mutation	p.Thr358Met(p.T358M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000374012
Start	35842670:35842670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.181G>A
AA Mutation	p.Asp61Asn(p.D61N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000374012
Start	35938930:35938930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148716053
CDS Mutation	c.2534G>A
AA Mutation	p.Arg845His(p.R845H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000374012
Start	35941012:35941012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776268666
CDS Mutation	c.2861C>T
AA Mutation	p.Thr954Met(p.T954M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000374012
Start	35917588:35917588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1930G>A
AA Mutation	p.Gly644Arg(p.G644R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374012
Start	35899554:35899554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs565748652
CDS Mutation	c.1467G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374012
Start	35863396:35863396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.804T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374012
Start	35913283:35913283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1596A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000374012
Start	35938869:35938869(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2476delC
AA Mutation	p.Leu826CysfsTer62(p.L826Cfs*62)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000374012
Start	35801596:35801597(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.80dupA
AA Mutation	p.Asn27LysfsTer11(p.N27Kfs*11)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> PHF20

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374012
Start	35869527:35869527(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762848107
CDS Mutation	c.898C>T
AA Mutation	p.Arg300Cys(p.R300C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374012
Start	35871818:35871818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780164709
CDS Mutation	c.1271C>T
AA Mutation	p.Ser424Leu(p.S424L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000374012
Start	35927857:35927857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2082T>G
AA Mutation	p.Cys694Trp(p.C694W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript