Colon Cancer: Gene >> KRT79

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000330553
Start	52823043:52823043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764247530
CDS Mutation	c.1340G>A
AA Mutation	p.Arg447His(p.R447H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000330553
Start	52823143:52823143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1240G>A
AA Mutation	p.Ala414Thr(p.A414T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000330553
Start	52823119:52823119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1264C>A
AA Mutation	p.Leu422Met(p.L422M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000330553
Start	52834242:52834242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.19C>T
AA Mutation	p.Arg7Trp(p.R7W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000330553
Start	52833789:52833789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs575190754
CDS Mutation	c.472G>A
AA Mutation	p.Asp158Asn(p.D158N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000330553
Start	52823103:52823103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775879705
CDS Mutation	c.1280G>A
AA Mutation	p.Arg427His(p.R427H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000330553
Start	52822068:52822068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1412G>A
AA Mutation	p.Gly471Asp(p.G471D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000330553
Start	52823195:52823195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1188T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000330553
Start	52823953:52823953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745617726
CDS Mutation	c.1080C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000330553
Start	52831567:52831567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.537G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000330553
Start	52821994:52821994(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs746321620
CDS Mutation	c.1486delG
AA Mutation	p.Ala496ProfsTer43(p.A496Pfs*43)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000330553
Start	52823190:52823191(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1192dupG
AA Mutation	p.Glu398GlyfsTer31(p.E398Gfs*31)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000330553
Start	52834000:52834001(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.260dupG
AA Mutation	p.Phe88LeufsTer45(p.F88Lfs*45)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000330553
Start	52831414:52831415(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.689_690insAGAGCTCAGAAACGTGCAGGACCTTGTGGAGGACTT
AA Mutation	p.Asp229_Phe230insLeuGluLeuArgAsnValGlnAspLeuValGluAsp(p.D229_F230insLELRNVQDLVED)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> KRT79

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000330553
Start	52834082:52834082(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765976515
CDS Mutation	c.179G>A
AA Mutation	p.Arg60Gln(p.R60Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000330553
Start	52830256:52830256(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.735G>T
AA Mutation	p.Glu245Asp(p.E245D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000330553
Start	52831601:52831601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.503A>C
AA Mutation	p.Lys168Thr(p.K168T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript