Colon Cancer: Gene >> PALM2-AKAP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374530
Start	109931975:109931975(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.443G>A
AA Mutation	p.Cys148Tyr(p.C148Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374530
Start	109925074:109925074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150674445
CDS Mutation	c.386C>T
AA Mutation	p.Thr129Met(p.T129M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000374530
Start	110137372:110137372(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1828C>T
AA Mutation	p.Pro610Ser(p.P610S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000374530
Start	110136706:110136706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1162A>T
AA Mutation	p.Thr388Ser(p.T388S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000374530
Start	110136781:110136781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753146690
CDS Mutation	c.1237C>T
AA Mutation	p.Arg413Cys(p.R413C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000374530
Start	110136206:110136206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.662C>T
AA Mutation	p.Ala221Val(p.A221V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000374530
Start	110168447:110168447(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370918671
CDS Mutation	c.3262C>T
AA Mutation	p.Arg1088Cys(p.R1088C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000374530
Start	110136795:110136795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1251G>C
AA Mutation	p.Glu417Asp(p.E417D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000374530
Start	110136889:110136889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776011217
CDS Mutation	c.1345C>G
AA Mutation	p.Leu449Val(p.L449V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000374530
Start	110168445:110168445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3260T>C
AA Mutation	p.Leu1087Ser(p.L1087S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374530
Start	110137248:110137248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1704G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374530
Start	110137365:110137365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142232519
CDS Mutation	c.1821C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374530
Start	110136345:110136345(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.801C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374530
Start	110136883:110136883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1339C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000374530
Start	110136907:110136907(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1363G>T
AA Mutation	p.Glu455Ter(p.E455*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> PALM2-AKAP2

No Mutation Annotation!