Colon Cancer: Gene >> STRA6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000323940
Start	74202263:74202263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5C>T
AA Mutation	p.Ser2Leu(p.S2L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000323940
Start	74180851:74180851(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs115331762
CDS Mutation	c.1771G>A
AA Mutation	p.Ala591Thr(p.A591T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000323940
Start	74180796:74180796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1826G>A
AA Mutation	p.Gly609Glu(p.G609E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000323940
Start	74183899:74183899(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1257T>G
AA Mutation	p.Cys419Trp(p.C419W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000323940
Start	74183900:74183900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1256G>A
AA Mutation	p.Cys419Tyr(p.C419Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000323940
Start	74180815:74180815(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1807delC
AA Mutation	p.Gln603ArgfsTer171(p.Q603Rfs*171)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained;frameshift_variant;splice_region_variant
Transcription ID	ENST00000323940
Start	74196146:74196147(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.267-3_267dupTAGC
AA Mutation	p.Pro90Ter(p.P90*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000323940
Start	74197425:74197425(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.181-2A>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000323940
Start	74195650:74195650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.430+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> STRA6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000323940
Start	74191208:74191208(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.824C>G
AA Mutation	p.Ala275Gly(p.A275G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000323940
Start	74202235:74202235(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.33C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000323940
Start	74180891:74180891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776349957
CDS Mutation	c.1731G>A
Mutation Classification	Silent
Feature Type	Transcript