Colon Cancer: Gene >> ZNF44

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356109
Start	12273770:12273770(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.629C>A
AA Mutation	p.Pro210His(p.P210H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356109
Start	12273351:12273351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1048A>G
AA Mutation	p.Ile350Val(p.I350V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000356109
Start	12273809:12273809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.590G>T
AA Mutation	p.Gly197Val(p.G197V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000356109
Start	12273552:12273552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.847C>T
AA Mutation	p.Pro283Ser(p.P283S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000356109
Start	12273992:12273992(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773512413
CDS Mutation	c.407G>A
AA Mutation	p.Arg136Gln(p.R136Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356109
Start	12273175:12273175(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1224T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356109
Start	12273610:12273610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.789T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356109
Start	12273163:12273163(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1236C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000356109
Start	12273633:12273633(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.766delT
AA Mutation	p.Trp256GlyfsTer34(p.W256Gfs*34)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000356109
Start	12273114:12273114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs567730246
CDS Mutation	c.1285C>T
AA Mutation	p.Arg429Ter(p.R429*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000356109
Start	12273695:12273696(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.703_704insTGCTTACATTC
AA Mutation	p.His235LeufsTer7(p.H235Lfs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ZNF44

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356109
Start	12273992:12273992(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773512413
CDS Mutation	c.407G>A
AA Mutation	p.Arg136Gln(p.R136Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356109
Start	12272632:12272632(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1767C>A
AA Mutation	p.Phe589Leu(p.F589L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000356109
Start	12272634:12272634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1765T>G
AA Mutation	p.Phe589Val(p.F589V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000356109
Start	12272490:12272490(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1909G>T
AA Mutation	p.Glu637Ter(p.E637*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript