Colon Cancer: Gene >> PRLHR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000239032
Start	118594320:118594320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.925G>A
AA Mutation	p.Asp309Asn(p.D309N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000239032
Start	118594265:118594265(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.980C>T
AA Mutation	p.Ser327Leu(p.S327L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000239032
Start	118594965:118594965(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.280G>A
AA Mutation	p.Val94Met(p.V94M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000239032
Start	118594205:118594205(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1040G>A
AA Mutation	p.Arg347His(p.R347H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000239032
Start	118595028:118595028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.217G>A
AA Mutation	p.Val73Met(p.V73M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000239032
Start	118594227:118594227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756981778
CDS Mutation	c.1018G>A
AA Mutation	p.Asp340Asn(p.D340N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000239032
Start	118594871:118594871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.374G>A
AA Mutation	p.Arg125His(p.R125H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000239032
Start	118595037:118595037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.208G>A
AA Mutation	p.Val70Met(p.V70M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000239032
Start	118594324:118594324(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.921C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000239032
Start	118594327:118594327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.918C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000239032
Start	118595131:118595131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759397071
CDS Mutation	c.114G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000239032
Start	118594366:118594366(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.879G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000239032
Start	118594570:118594570(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.675C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000239032
Start	118594167:118594167(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1078delC
AA Mutation	p.His360MetfsTer5(p.H360Mfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PRLHR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000239032
Start	118594205:118594205(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1040G>A
AA Mutation	p.Arg347His(p.R347H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000239032
Start	118594802:118594802(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.443C>T
AA Mutation	p.Ser148Leu(p.S148L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript