Colon Cancer: Gene >> ANGPTL7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376819
Start	11194938:11194938(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.956G>A
AA Mutation	p.Gly319Asp(p.G319D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000376819
Start	11189848:11189848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753003549
CDS Mutation	c.269G>A
AA Mutation	p.Arg90His(p.R90H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000376819
Start	11189859:11189859(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771394500
CDS Mutation	c.280C>T
AA Mutation	p.Arg94Trp(p.R94W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000376819
Start	11194580:11194580(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.792G>C
AA Mutation	p.Gln264His(p.Q264H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000376819
Start	11189952:11189952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs577777414
CDS Mutation	c.373G>A
AA Mutation	p.Ala125Thr(p.A125T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000376819
Start	11192332:11192332(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.439C>A
AA Mutation	p.Leu147Ile(p.L147I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000376819
Start	11192312:11192312(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs28991002
CDS Mutation	c.419G>A
AA Mutation	p.Arg140His(p.R140H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376819
Start	11189933:11189933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.354G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ANGPTL7

No Mutation Annotation!