Colon Cancer: Gene >> VNN2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000326499
Start	132751211:132751211(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1134G>T
AA Mutation	p.Glu378Asp(p.E378D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000326499
Start	132752572:132752572(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.715A>C
AA Mutation	p.Met239Leu(p.M239L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000326499
Start	132752658:132752658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139095644
CDS Mutation	c.629C>T
AA Mutation	p.Thr210Met(p.T210M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000326499
Start	132749724:132749724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1342G>A
AA Mutation	p.Glu448Lys(p.E448K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326499
Start	132755921:132755921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.459T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326499
Start	132749713:132749713(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1353G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326499
Start	132752684:132752684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141716354
CDS Mutation	c.603C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326499
Start	132751412:132751412(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146263625
CDS Mutation	c.933G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326499
Start	132757686:132757686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.198G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326499
Start	132744488:132744488(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774067588
CDS Mutation	c.1375C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326499
Start	132755855:132755855(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.525A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000326499
Start	132744454:132744454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1409C>A
AA Mutation	p.Ser470Ter(p.S470*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000326499
Start	132751211:132751213(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1132_1134delGAG
AA Mutation	p.Glu378del(p.E378del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> VNN2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000326499
Start	132751204:132751204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1141G>T
AA Mutation	p.Val381Leu(p.V381L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000326499
Start	132751447:132751447(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.898C>A
AA Mutation	p.Leu300Ile(p.L300I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript