Colon Cancer: Gene >> FANCB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000324138
Start	14845236:14845236(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1547C>A
AA Mutation	p.Ser516Tyr(p.S516Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000324138
Start	14864864:14864864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.647C>T
AA Mutation	p.Ser216Phe(p.S216F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000324138
Start	14843749:14843749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2398G>A
AA Mutation	p.Ala800Thr(p.A800T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000324138
Start	14865161:14865161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.350A>C
AA Mutation	p.Lys117Thr(p.K117T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324138
Start	14844670:14844670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1998C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324138
Start	14844983:14844983(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1800A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324138
Start	14864614:14864614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753443421
CDS Mutation	c.897C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324138
Start	14844529:14844529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2139C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000324138
Start	14865196:14865196(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.315delT
AA Mutation	p.Phe105LeufsTer6(p.F105Lfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000324138
Start	14853109:14853110(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1255_1256insCT
AA Mutation	p.Ile419ThrfsTer9(p.I419Tfs*9)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000324138
Start	14853110:14853111(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1254_1255insCTAATATTCCAATTTAAATA
AA Mutation	p.Ile419LeufsTer7(p.I419Lfs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> FANCB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000324138
Start	14864729:14864729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.782G>A
AA Mutation	p.Arg261Gln(p.R261Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000324138
Start	14864628:14864628(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.883G>T
AA Mutation	p.Gly295Ter(p.G295*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript