Colon Cancer: Gene >> ALB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000295897
Start	73404398:73404398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs74821926
CDS Mutation	c.71G>A
AA Mutation	p.Arg24Gln(p.R24Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000295897
Start	73410324:73410324(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs267600248
CDS Mutation	c.628C>T
AA Mutation	p.Arg210Trp(p.R210W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000295897
Start	73410372:73410372(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.676A>G
AA Mutation	p.Ser226Gly(p.S226G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000295897
Start	73409367:73409367(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.495A>C
AA Mutation	p.Glu165Asp(p.E165D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000295897
Start	73418131:73418131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776185501
CDS Mutation	c.1472C>T
AA Mutation	p.Thr491Met(p.T491M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000295897
Start	73413457:73413457(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774294755
CDS Mutation	c.881C>T
AA Mutation	p.Ser294Leu(p.S294L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295897
Start	73408785:73408785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.462T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295897
Start	73412020:73412020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.738A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000295897
Start	73417606:73417606(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1368delA
AA Mutation	p.Val457TrpfsTer25(p.V457Wfs*25)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000295897
Start	73418313:73418313(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1652+2delT
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> ALB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000295897
Start	73410405:73410405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.709G>A
AA Mutation	p.Ala237Thr(p.A237T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000295897
Start	73419636:73419636(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1782G>T
AA Mutation	p.Glu594Asp(p.E594D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000295897
Start	73410343:73410343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.647C>T
AA Mutation	p.Ser216Leu(p.S216L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295897
Start	73419579:73419579(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1725C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295897
Start	73409451:73409451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.579C>T
Mutation Classification	Silent
Feature Type	Transcript