Colon Cancer: Gene >> SP3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000310015
Start	173955695:173955695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.817G>A
AA Mutation	p.Asp273Asn(p.D273N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000310015
Start	173913114:173913114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1985T>G
AA Mutation	p.Phe662Cys(p.F662C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000310015
Start	173918639:173918639(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753208366
CDS Mutation	c.1786C>T
AA Mutation	p.Arg596Trp(p.R596W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000310015
Start	173913133:173913133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1966A>G
AA Mutation	p.Met656Val(p.M656V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000310015
Start	173913117:173913117(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1982G>T
AA Mutation	p.Arg661Ile(p.R661I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000310015
Start	173954891:173954891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1621A>G
AA Mutation	p.Asn541Asp(p.N541D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000310015
Start	173910138:173910138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2149G>A
AA Mutation	p.Ala717Thr(p.A717T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310015
Start	173918691:173918691(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1734A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310015
Start	173955636:173955636(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.876C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310015
Start	173956203:173956203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.309A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310015
Start	173955387:173955387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1125G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310015
Start	173955009:173955009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs189281761
CDS Mutation	c.1503G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000310015
Start	173955815:173955819(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.693_697delTGGTC
AA Mutation	p.Gly232SerfsTer22(p.G232Sfs*22)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000310015
Start	173910166:173910166(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2121delA
AA Mutation	p.Gly708ValfsTer20(p.G708Vfs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000310015
Start	173955548:173955548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.964G>T
AA Mutation	p.Glu322Ter(p.E322*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000310015
Start	173955428:173955428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1084C>T
AA Mutation	p.Gln362Ter(p.Q362*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SP3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000310015
Start	173955695:173955695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.817G>A
AA Mutation	p.Asp273Asn(p.D273N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000310015
Start	173913153:173913153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1946G>A
AA Mutation	p.Arg649His(p.R649H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript