Colon Cancer: Gene >> GPER1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000297469
Start	1092470:1092470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775750584
CDS Mutation	c.742C>T
AA Mutation	p.Arg248Cys(p.R248C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000297469
Start	1092314:1092314(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.586G>A
AA Mutation	p.Val196Met(p.V196M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000297469
Start	1091980:1091980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.252C>A
AA Mutation	p.Asn84Lys(p.N84K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000297469
Start	1091756:1091756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs61735233
CDS Mutation	c.28G>A
AA Mutation	p.Val10Met(p.V10M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000297469
Start	1091795:1091795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.67G>C
AA Mutation	p.Ala23Pro(p.A23P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000297469
Start	1092585:1092585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs569932251
CDS Mutation	c.857G>A
AA Mutation	p.Arg286Gln(p.R286Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000297469
Start	1091784:1091784(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779447108
CDS Mutation	c.56C>T
AA Mutation	p.Ala19Val(p.A19V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000297469
Start	1092218:1092218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.490C>T
AA Mutation	p.Arg164Cys(p.R164C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297469
Start	1092550:1092550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369986460
CDS Mutation	c.822G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297469
Start	1092556:1092556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200314011
CDS Mutation	c.828C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297469
Start	1092007:1092007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149535499
CDS Mutation	c.279C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> GPER1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297469
Start	1092160:1092160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143366301
CDS Mutation	c.432C>T
Mutation Classification	Silent
Feature Type	Transcript