Colon Cancer: Gene >> MAPKAP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265960
Start	125669846:125669846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.321G>C
AA Mutation	p.Gln107His(p.Q107H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265960
Start	125585570:125585570(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747216426
CDS Mutation	c.656G>A
AA Mutation	p.Arg219Gln(p.R219Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265960
Start	125559636:125559636(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.845G>A
AA Mutation	p.Arg282Gln(p.R282Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265960
Start	125506373:125506373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145885264
CDS Mutation	c.1003G>A
AA Mutation	p.Val335Ile(p.V335I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265960
Start	125585694:125585694(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.532G>A
AA Mutation	p.Asp178Asn(p.D178N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000265960
Start	125672465:125672465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.110A>G
AA Mutation	p.Asp37Gly(p.D37G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000265960
Start	125444535:125444535(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1409C>T
AA Mutation	p.Ser470Leu(p.S470L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000265960
Start	125669835:125669835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.332G>T
AA Mutation	p.Arg111Ile(p.R111I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265960
Start	125585644:125585644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766213534
CDS Mutation	c.582C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265960
Start	125585578:125585578(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.648C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265960
Start	125438926:125438926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1530C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> MAPKAP1

No Mutation Annotation!