Colon Cancer: Gene >> COL8A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261037
Start	99794269:99794269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769320857
CDS Mutation	c.368G>A
AA Mutation	p.Arg123His(p.R123H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261037
Start	99794268:99794268(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745489693
CDS Mutation	c.367C>T
AA Mutation	p.Arg123Cys(p.R123C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261037
Start	99796086:99796086(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762335752
CDS Mutation	c.2185G>A
AA Mutation	p.Gly729Arg(p.G729R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261037
Start	99794362:99794362(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.461A>G
AA Mutation	p.Tyr154Cys(p.Y154C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261037
Start	99790693:99790693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.11T>G
AA Mutation	p.Leu4Arg(p.L4R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000261037
Start	99796039:99796039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2138G>T
AA Mutation	p.Arg713Leu(p.R713L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000261037
Start	99790987:99790987(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.305A>G
AA Mutation	p.Glu102Gly(p.E102G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261037
Start	99794429:99794429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.528G>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261037
Start	99794915:99794915(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1014G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261037
Start	99795296:99795296(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1395G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261037
Start	99794858:99794858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.957C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261037
Start	99795824:99795824(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773581749
CDS Mutation	c.1923C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261037
Start	99795953:99795953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2052C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261037
Start	99795690:99795690(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1795delC
AA Mutation	p.His599MetfsTer24(p.H599Mfs*24)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261037
Start	99795422:99795422(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1524delC
AA Mutation	p.Ile509LeufsTer24(p.I509Lfs*24)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261037
Start	99795624:99795624(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1727delC
AA Mutation	p.Pro576LeufsTer20(p.P576Lfs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000261037
Start	99794439:99794439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.538G>T
AA Mutation	p.Glu180Ter(p.E180*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> COL8A1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261037
Start	99794954:99794954(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1053G>A
Mutation Classification	Silent
Feature Type	Transcript