Colon Cancer: Gene >> PHLDB3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000292140
Start	43475420:43475420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1913A>G
AA Mutation	p.His638Arg(p.H638R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000292140
Start	43494752:43494752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1099G>A
AA Mutation	p.Ala367Thr(p.A367T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000292140
Start	43478060:43478060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367616579
CDS Mutation	c.1775G>A
AA Mutation	p.Arg592His(p.R592H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000292140
Start	43501751:43501751(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148749895
CDS Mutation	c.517C>T
AA Mutation	p.Arg173Cys(p.R173C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000292140
Start	43479525:43479525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1554G>T
AA Mutation	p.Trp518Cys(p.W518C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000292140
Start	43502166:43502166(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147272153
CDS Mutation	c.331C>T
AA Mutation	p.Arg111Cys(p.R111C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000292140
Start	43497210:43497210(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.733A>G
AA Mutation	p.Ser245Gly(p.S245G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000292140
Start	43502203:43502203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.294G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000292140
Start	43487048:43487048(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1225delC
AA Mutation	p.Arg409AspfsTer32(p.R409Dfs*32)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PHLDB3

No Mutation Annotation!