Colon Cancer: Gene >> ASS1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000352480
Start	130458548:130458548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143405567
CDS Mutation	c.322C>T
AA Mutation	p.Arg108Trp(p.R108W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000352480
Start	130489350:130489350(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.856G>A
AA Mutation	p.Ala286Thr(p.A286T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000352480
Start	130466744:130466744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.440T>C
AA Mutation	p.Met147Thr(p.M147T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000352480
Start	130489413:130489413(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs183276875
CDS Mutation	c.919C>T
AA Mutation	p.Arg307Cys(p.R307C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000352480
Start	130489340:130489340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs549085827
CDS Mutation	c.846C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000352480
Start	130458511:130458511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.285G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000352480
Start	130494904:130494904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1008C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000352480
Start	130464154:130464154(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.412delC
AA Mutation	p.Gln138ArgfsTer2(p.Q138Rfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ASS1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000352480
Start	130476910:130476910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.637C>G
AA Mutation	p.Pro213Ala(p.P213A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000352480
Start	130479744:130479744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.717G>T
AA Mutation	p.Lys239Asn(p.K239N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000352480
Start	130476912:130476912(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.639A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000352480
Start	130470872:130470872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs113818350
CDS Mutation	c.534G>A
Mutation Classification	Silent
Feature Type	Transcript