Colon Cancer: Gene >> ADSL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000623063
Start	40349907:40349907(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775646855
CDS Mutation	c.229G>A
AA Mutation	p.Ala77Thr(p.A77T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000623063
Start	40363031:40363031(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752238667
CDS Mutation	c.1061C>T
AA Mutation	p.Thr354Met(p.T354M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000623063
Start	40361589:40361589(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.964G>A
AA Mutation	p.Ala322Thr(p.A322T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000623063
Start	40364316:40364316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1142C>T
AA Mutation	p.Ala381Val(p.A381V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000623063
Start	40364893:40364893(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1205A>C
AA Mutation	p.Lys402Thr(p.K402T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000623063
Start	40358916:40358916(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.535C>A
AA Mutation	p.Leu179Ile(p.L179I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000623063
Start	40361610:40361610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370221257
CDS Mutation	c.985C>T
AA Mutation	p.Arg329Cys(p.R329C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000623063
Start	40361497:40361497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.872C>T
AA Mutation	p.Ala291Val(p.A291V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000623063
Start	40349895:40349895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745787396
CDS Mutation	c.217G>A
AA Mutation	p.Asp73Asn(p.D73N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000623063
Start	40362992:40362992(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1022T>G
AA Mutation	p.Leu341Trp(p.L341W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000623063
Start	40358891:40358891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.510A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000623063
Start	40366489:40366489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748593655
CDS Mutation	c.1422C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000623063
Start	40358871:40358871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.490C>T
AA Mutation	p.Gln164Ter(p.Q164*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ADSL

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000623063
Start	40349894:40349894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145786986
CDS Mutation	c.216C>T
Mutation Classification	Silent
Feature Type	Transcript