Colon Cancer: Gene >> BAIAP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000321300
Start	81085688:81085688(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.314T>C
AA Mutation	p.Leu105Pro(p.L105P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000321300
Start	81104676:81104676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1229G>A
AA Mutation	p.Arg410His(p.R410H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000321300
Start	81106815:81106815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768070859
CDS Mutation	c.1408G>A
AA Mutation	p.Asp470Asn(p.D470N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000321300
Start	81104619:81104619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1172G>A
AA Mutation	p.Ser391Asn(p.S391N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000321300
Start	81057942:81057942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372246311
CDS Mutation	c.192C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000321300
Start	81086565:81086565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776492137
CDS Mutation	c.474G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000321300
Start	81106809:81106809(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1407delC
AA Mutation	p.Asp470IlefsTer41(p.D470Ifs*41)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> BAIAP2

No Mutation Annotation!