Colon Cancer: Gene >> ALDH1B1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377698
Start	38395887:38395887(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.139G>A
AA Mutation	p.Asp47Asn(p.D47N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377698
Start	38396464:38396464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779633928
CDS Mutation	c.716C>T
AA Mutation	p.Thr239Met(p.T239M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000377698
Start	38396878:38396878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1130G>A
AA Mutation	p.Gly377Asp(p.G377D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000377698
Start	38397085:38397085(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752017437
CDS Mutation	c.1337C>T
AA Mutation	p.Ala446Val(p.A446V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000377698
Start	38395756:38395756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775731660
CDS Mutation	c.8G>A
AA Mutation	p.Arg3His(p.R3H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000377698
Start	38396056:38396056(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755939166
CDS Mutation	c.308G>A
AA Mutation	p.Arg103Gln(p.R103Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000377698
Start	38395800:38395800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.52C>A
AA Mutation	p.Arg18Ser(p.R18S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000377698
Start	38396980:38396980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1232G>T
AA Mutation	p.Arg411Ile(p.R411I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377698
Start	38396963:38396963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs535405575
CDS Mutation	c.1215C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377698
Start	38397143:38397143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765513995
CDS Mutation	c.1395C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000377698
Start	38396389:38396389(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.646delC
AA Mutation	p.Leu216SerfsTer20(p.L216Sfs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000377698
Start	38396832:38396833(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1085_1086delTG
AA Mutation	p.Val362GlyfsTer6(p.V362Gfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ALDH1B1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377698
Start	38396269:38396269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.521A>C
AA Mutation	p.Glu174Ala(p.E174A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377698
Start	38395988:38395988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.240G>T
Mutation Classification	Silent
Feature Type	Transcript