Colon Cancer: Gene >> VPS37B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000267202
Start	122867457:122867457(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.517C>A
AA Mutation	p.Leu173Met(p.L173M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000267202
Start	122867160:122867160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.814C>T
AA Mutation	p.Pro272Ser(p.P272S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000267202
Start	122867252:122867252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370211610
CDS Mutation	c.722C>T
AA Mutation	p.Pro241Leu(p.P241L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000267202
Start	122868497:122868497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.349A>G
AA Mutation	p.Ile117Val(p.I117V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000267202
Start	122867494:122867494(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.480G>T
AA Mutation	p.Gln160His(p.Q160H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000267202
Start	122870958:122870958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761502771
CDS Mutation	c.215G>A
AA Mutation	p.Arg72His(p.R72H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000267202
Start	122867416:122867416(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765717985
CDS Mutation	c.558C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000267202
Start	122867347:122867347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368470573
CDS Mutation	c.627C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000267202
Start	122867238:122867238(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.736delC
AA Mutation	p.Arg246AlafsTer91(p.R246Afs*91)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> VPS37B

No Mutation Annotation!