Colon Cancer: Gene >> GPR182

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000300098
Start	56995695:56995695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.486G>T
AA Mutation	p.Trp162Cys(p.W162C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000300098
Start	56995502:56995502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746296301
CDS Mutation	c.293C>T
AA Mutation	p.Ala98Val(p.A98V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000300098
Start	56996246:56996246(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760425192
CDS Mutation	c.1037C>T
AA Mutation	p.Ala346Val(p.A346V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000300098
Start	56995342:56995342(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753611146
CDS Mutation	c.133G>A
AA Mutation	p.Val45Met(p.V45M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000300098
Start	56995859:56995859(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368453485
CDS Mutation	c.650C>T
AA Mutation	p.Ala217Val(p.A217V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300098
Start	56995938:56995938(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.729C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300098
Start	56995257:56995257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs565165510
CDS Mutation	c.48C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> GPR182

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000300098
Start	56995846:56995846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.637A>T
AA Mutation	p.Thr213Ser(p.T213S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript