Colon Cancer: Gene >> DAPK2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261891
Start	63971539:63971539(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs553988389
CDS Mutation	c.337G>A
AA Mutation	p.Asp113Asn(p.D113N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261891
Start	64040208:64040208(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.54G>C
AA Mutation	p.Lys18Asn(p.K18N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261891
Start	63929567:63929567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140850258
CDS Mutation	c.643G>A
AA Mutation	p.Val215Ile(p.V215I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261891
Start	64040225:64040225(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.37C>T
AA Mutation	p.Pro13Ser(p.P13S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261891
Start	63925965:63925965(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749221840
CDS Mutation	c.788G>A
AA Mutation	p.Arg263Gln(p.R263Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261891
Start	63983574:63983574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201638173
CDS Mutation	c.273C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261891
Start	63912126:63912126(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.930T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261891
Start	63939245:63939245(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.570G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261891
Start	64040208:64040208(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149132625
CDS Mutation	c.54G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261891
Start	63926076:63926076(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.677delC
AA Mutation	p.Pro226LeufsTer17(p.P226Lfs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> DAPK2

No Mutation Annotation!