Colon Cancer: Gene >> ASPRV1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000320256
Start	69961069:69961069(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.620T>C
AA Mutation	p.Val207Ala(p.V207A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000320256
Start	69961130:69961130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371446435
CDS Mutation	c.559G>A
AA Mutation	p.Val187Ile(p.V187I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000320256
Start	69960995:69960995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747852584
CDS Mutation	c.694G>A
AA Mutation	p.Asp232Asn(p.D232N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000320256
Start	69961336:69961336(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.353A>G
AA Mutation	p.His118Arg(p.H118R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000320256
Start	69961107:69961107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.582G>T
AA Mutation	p.Lys194Asn(p.K194N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000320256
Start	69961385:69961385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149847323
CDS Mutation	c.304G>A
AA Mutation	p.Val102Ile(p.V102I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000320256
Start	69961380:69961380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762805708
CDS Mutation	c.309G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000320256
Start	69960978:69960978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.711G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000320256
Start	69960882:69960882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.807G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000320256
Start	69960821:69960821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.868C>T
AA Mutation	p.Gln290Ter(p.Q290*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000320256
Start	69960725:69960725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.964G>T
AA Mutation	p.Glu322Ter(p.E322*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ASPRV1

No Mutation Annotation!