Colon Cancer: Gene >> RORC

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000318247
Start	151816684:151816684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs546157871
CDS Mutation	c.278C>T
AA Mutation	p.Ala93Val(p.A93V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000318247
Start	151814999:151814999(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.725G>T
AA Mutation	p.Gly242Val(p.G242V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000318247
Start	151815414:151815414(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.310G>A
AA Mutation	p.Gly104Ser(p.G104S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318247
Start	151817237:151817237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201478663
CDS Mutation	c.114G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318247
Start	151813591:151813591(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.963C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318247
Start	151807553:151807553(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755666505
CDS Mutation	c.1476C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000318247
Start	151815202:151815203(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.521dupC
AA Mutation	p.Gly175TrpfsTer29(p.G175Wfs*29)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000318247
Start	151816738:151816739(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.223dupA
AA Mutation	p.Ile75AsnfsTer91(p.I75Nfs*91)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> RORC

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000318247
Start	151815069:151815069(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.655A>G
AA Mutation	p.Ser219Gly(p.S219G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000318247
Start	151816733:151816733(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.229C>T
AA Mutation	p.Arg77Cys(p.R77C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript