Colon Cancer: Gene >> ZNF625

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000439556
Start	12146205:12146205(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.211C>A
AA Mutation	p.Leu71Ile(p.L71I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000439556
Start	12145768:12145768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.648G>T
AA Mutation	p.Glu216Asp(p.E216D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000439556
Start	12147430:12147430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.156T>G
AA Mutation	p.Ile52Met(p.I52M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000439556
Start	12145712:12145712(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750463530
CDS Mutation	c.704G>A
AA Mutation	p.Arg235Gln(p.R235Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000439556
Start	12145700:12145700(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.716G>T
AA Mutation	p.Arg239Ile(p.R239I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000439556
Start	12145669:12145669(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.747C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000439556
Start	12145936:12145936(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.480delG
AA Mutation	p.Lys161AsnfsTer23(p.K161Nfs*23)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000439556
Start	12145345:12145345(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1071delA
AA Mutation	p.Lys357AsnfsTer?(p.K357Nfs*?)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained;frameshift_variant
Transcription ID	ENST00000439556
Start	12145423:12145424(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.992_993insGGAATCTTATG
AA Mutation	p.Tyr331Ter(p.Y331*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000439556
Start	12145965:12145965(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.451C>T
AA Mutation	p.Arg151Ter(p.R151*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000439556
Start	12147447:12147448(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.138dupA
AA Mutation	p.Trp47MetfsTer7(p.W47Mfs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ZNF625

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000439556
Start	12145460:12145460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749361928
CDS Mutation	c.956G>A
AA Mutation	p.Arg319Gln(p.R319Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000439556
Start	12145325:12145325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140651282
CDS Mutation	c.1091C>T
AA Mutation	p.Ser364Leu(p.S364L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000439556
Start	12145712:12145712(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750463530
CDS Mutation	c.704G>A
AA Mutation	p.Arg235Gln(p.R235Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000439556
Start	12146017:12146017(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.399G>A
Mutation Classification	Silent
Feature Type	Transcript