Colon Cancer: Gene >> NPLOC4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000331134
Start	81597265:81597265(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763449135
CDS Mutation	c.973G>A
AA Mutation	p.Val325Ile(p.V325I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000331134
Start	81606762:81606762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758048463
CDS Mutation	c.583G>A
AA Mutation	p.Glu195Lys(p.E195K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000331134
Start	81622214:81622214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.161G>A
AA Mutation	p.Gly54Glu(p.G54E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000331134
Start	81610253:81610253(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.392G>A
AA Mutation	p.Arg131His(p.R131H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331134
Start	81588992:81588992(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368218835
CDS Mutation	c.1233C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331134
Start	81613416:81613416(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.288C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331134
Start	81604641:81604641(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.741G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331134
Start	81608763:81608763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200088672
CDS Mutation	c.495C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000331134
Start	81604635:81604635(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.747delT
AA Mutation	p.Phe249LeufsTer88(p.F249Lfs*88)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> NPLOC4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000331134
Start	81597252:81597252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.986G>A
AA Mutation	p.Arg329Gln(p.R329Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000331134
Start	81604700:81604700(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.682T>C
AA Mutation	p.Phe228Leu(p.F228L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript