Colon Cancer: Gene >> ALDH1A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000297785
Start	72912065:72912065(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1093G>A
AA Mutation	p.Gly365Arg(p.G365R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000297785
Start	72928943:72928943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371735738
CDS Mutation	c.391C>T
AA Mutation	p.Arg131Cys(p.R131C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000297785
Start	72912013:72912013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1145T>C
AA Mutation	p.Val382Ala(p.V382A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000297785
Start	72901278:72901278(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1436G>T
AA Mutation	p.Gly479Val(p.G479V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000297785
Start	72911975:72911975(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762664992
CDS Mutation	c.1183C>T
AA Mutation	p.Arg395Cys(p.R395C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000297785
Start	72925548:72925548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.569T>A
AA Mutation	p.Val190Glu(p.V190E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000297785
Start	72909623:72909623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs1803054
CDS Mutation	c.1337C>A
AA Mutation	p.Ala446Asp(p.A446D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000297785
Start	72909756:72909756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1204T>G
AA Mutation	p.Phe402Val(p.F402V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297785
Start	72905999:72905999(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1392C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297785
Start	72930942:72930942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.249C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ALDH1A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000297785
Start	72909685:72909685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1275C>A
AA Mutation	p.Phe425Leu(p.F425L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000297785
Start	72925569:72925569(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.548C>A
AA Mutation	p.Ala183Glu(p.A183E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript