Mutation

Primary Site >> Liver Cancer

Gene >> MAP2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000360351
Start	209710163:209710163(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4982G>A
AA Mutation	p.Arg1661Gln(p.R1661Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000360351
Start	209694515:209694515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2345C>A
AA Mutation	p.Ala782Glu(p.A782E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000360351
Start	209693501:209693501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1331T>C
AA Mutation	p.Leu444Pro(p.L444P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000360351
Start	209695763:209695763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3593A>T
AA Mutation	p.Gln1198Leu(p.Q1198L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000360351
Start	209694644:209694644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780854358
CDS Mutation	c.2474A>G
AA Mutation	p.Asp825Gly(p.D825G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000360351
Start	209697039:209697039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4510C>T
AA Mutation	p.Arg1504Trp(p.R1504W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000360351
Start	209695107:209695107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2937A>T
AA Mutation	p.Lys979Asn(p.K979N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000360351
Start	209695646:209695646(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3476C>G
AA Mutation	p.Ser1159Cys(p.S1159C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360351
Start	209695966:209695966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3796A>C
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360351
Start	209695926:209695926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3756A>T
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360351
Start	209693028:209693028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.858T>A
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360351
Start	209653275:209653275(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.105C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360351
Start	209729890:209729890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5196C>T
Mutation Classification	Silent
Feature Type	Transcript