Colon Cancer: Gene >> CD19

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000324662
Start	28932418:28932418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150438147
CDS Mutation	c.161G>T
AA Mutation	p.Arg54Leu(p.R54L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000324662
Start	28938943:28938943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1651G>T
AA Mutation	p.Gly551Cys(p.G551C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000324662
Start	28933468:28933468(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.794A>G
AA Mutation	p.Asn265Ser(p.N265S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000324662
Start	28937332:28937332(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747967568
CDS Mutation	c.1260C>A
AA Mutation	p.Phe420Leu(p.F420L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000324662
Start	28935488:28935488(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.880G>A
AA Mutation	p.Ala294Thr(p.A294T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000324662
Start	28932477:28932477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.220C>T
AA Mutation	p.His74Tyr(p.H74Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000324662
Start	28932487:28932487(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.230C>A
AA Mutation	p.Pro77His(p.P77H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000324662
Start	28936567:28936567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148576690
CDS Mutation	c.1051G>A
AA Mutation	p.Val351Met(p.V351M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000324662
Start	28937128:28937128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757806171
CDS Mutation	c.1190C>T
AA Mutation	p.Pro397Leu(p.P397L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324662
Start	28932984:28932984(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.429C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324662
Start	28935484:28935484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.876C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324662
Start	28932936:28932936(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142342927
CDS Mutation	c.381G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324662
Start	28937099:28937099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1161G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324662
Start	28937368:28937368(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1296C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000324662
Start	28932558:28932558(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.306delC
AA Mutation	p.Ser103LeufsTer27(p.S103Lfs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000324662
Start	28938718:28938718(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1534delC
AA Mutation	p.Gln512SerfsTer67(p.Q512Sfs*67)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CD19

No Mutation Annotation!