Colon Cancer: Gene >> ALDOB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374855
Start	101424898:101424898(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.944G>C
AA Mutation	p.Gly315Ala(p.G315A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374855
Start	101426595:101426595(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.584G>A
AA Mutation	p.Gly195Glu(p.G195E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000374855
Start	101427540:101427540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.482G>T
AA Mutation	p.Ser161Ile(p.S161I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000374855
Start	101425537:101425537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775786023
CDS Mutation	c.715G>T
AA Mutation	p.Ala239Ser(p.A239S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000374855
Start	101424926:101424926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.916C>A
AA Mutation	p.Leu306Met(p.L306M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000374855
Start	101427535:101427535(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs17852652
CDS Mutation	c.487G>A
AA Mutation	p.Ala163Thr(p.A163T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000374855
Start	101429809:101429809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.270G>T
AA Mutation	p.Gln90His(p.Q90H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000374855
Start	101429912:101429912(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200050226
CDS Mutation	c.167G>A
AA Mutation	p.Arg56His(p.R56H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374855
Start	101429857:101429857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754735910
CDS Mutation	c.222C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374855
Start	101421839:101421839(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1065G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000374855
Start	101428485:101428488(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs762198323
CDS Mutation	c.360_363delCAAA
AA Mutation	p.Asn120LysfsTer32(p.N120Kfs*32)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ALDOB

No Mutation Annotation!