Colon Cancer: Gene >> GALR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000299727
Start	77250831:77250831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.283G>A
AA Mutation	p.Val95Met(p.V95M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000299727
Start	77251140:77251140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.592A>C
AA Mutation	p.Lys198Gln(p.K198Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000299727
Start	77250747:77250747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.199C>T
AA Mutation	p.Arg67Trp(p.R67W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000299727
Start	77250946:77250946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.398G>A
AA Mutation	p.Arg133His(p.R133H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000299727
Start	77250987:77250987(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.439A>G
AA Mutation	p.Arg147Gly(p.R147G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000299727
Start	77268714:77268714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149816752
CDS Mutation	c.862G>A
AA Mutation	p.Ala288Thr(p.A288T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299727
Start	77268824:77268824(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.972A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299727
Start	77250596:77250596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.48G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299727
Start	77250650:77250650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.102C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299727
Start	77251052:77251052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149293813
CDS Mutation	c.504G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299727
Start	77251163:77251163(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.615C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000299727
Start	77251068:77251068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.520C>T
AA Mutation	p.Gln174Ter(p.Q174*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> GALR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000299727
Start	77268825:77268825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.973G>T
AA Mutation	p.Asp325Tyr(p.D325Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000299727
Start	77268849:77268849(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.997G>T
AA Mutation	p.Glu333Ter(p.E333*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript