Colon Cancer: Gene >> ANXA11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372231
Start	80157977:80157977(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1325A>C
AA Mutation	p.Lys442Thr(p.K442T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000372231
Start	80157676:80157676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368132715
CDS Mutation	c.1423C>T
AA Mutation	p.Arg475Trp(p.R475W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000372231
Start	80157675:80157675(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146644733
CDS Mutation	c.1424G>A
AA Mutation	p.Arg475Gln(p.R475Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000372231
Start	80169187:80169187(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.343T>A
AA Mutation	p.Ser115Thr(p.S115T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000372231
Start	80170834:80170834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762084152
CDS Mutation	c.137C>T
AA Mutation	p.Ala46Val(p.A46V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372231
Start	80168987:80168987(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.543C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372231
Start	80164105:80164105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773985331
CDS Mutation	c.897C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000372231
Start	80169122:80169122(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs771435989
CDS Mutation	c.408delC
AA Mutation	p.Gly137AspfsTer14(p.G137Dfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000372231
Start	80164128:80164128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.874G>T
AA Mutation	p.Glu292Ter(p.E292*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000372231
Start	80166198:80166198(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.745-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> ANXA11

No Mutation Annotation!