Colon Cancer: Gene >> ALS2CR12

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000286190
Start	201288771:201288771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1222A>C
AA Mutation	p.Ile408Leu(p.I408L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000286190
Start	201288767:201288767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1226C>A
AA Mutation	p.Ser409Tyr(p.S409Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000286190
Start	201342403:201342403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.491C>T
AA Mutation	p.Ala164Val(p.A164V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000286190
Start	201309179:201309179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs528302046
CDS Mutation	c.747C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000286190
Start	201307600:201307600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766784931
CDS Mutation	c.798C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ALS2CR12

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000286190
Start	201346638:201346638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774443454
CDS Mutation	c.272G>A
AA Mutation	p.Arg91Gln(p.R91Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000286190
Start	201299259:201299259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.921A>T
AA Mutation	p.Glu307Asp(p.E307D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000286190
Start	201307600:201307600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766784931
CDS Mutation	c.798C>T
Mutation Classification	Silent
Feature Type	Transcript