Colon Cancer: Gene >> PRICKLE1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000345127
Start	42460261:42460261(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768954477
CDS Mutation	c.2044C>T
AA Mutation	p.Arg682Cys(p.R682C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000345127
Start	42460240:42460240(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2065C>A
AA Mutation	p.Leu689Ile(p.L689I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000345127
Start	42464524:42464524(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1510C>A
AA Mutation	p.His504Asn(p.H504N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000345127
Start	42469485:42469485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.349C>A
AA Mutation	p.Leu117Met(p.L117M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000345127
Start	42459870:42459870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2435A>G
AA Mutation	p.Gln812Arg(p.Q812R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000345127
Start	42466376:42466376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.593T>G
AA Mutation	p.Ile198Ser(p.I198S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000345127
Start	42460279:42460279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779314205
CDS Mutation	c.2026C>T
AA Mutation	p.Arg676Trp(p.R676W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000345127
Start	42460175:42460175(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2130G>T
AA Mutation	p.Glu710Asp(p.E710D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000345127
Start	42466263:42466263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372213429
CDS Mutation	c.706C>T
AA Mutation	p.Arg236Cys(p.R236C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000345127
Start	42466226:42466226(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.743C>T
AA Mutation	p.Ala248Val(p.A248V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000345127
Start	42465048:42465048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.986A>G
AA Mutation	p.Asp329Gly(p.D329G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000345127
Start	42460122:42460122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2183C>A
AA Mutation	p.Ala728Asp(p.A728D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000345127
Start	42460335:42460335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1970G>A
AA Mutation	p.Arg657Gln(p.R657Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000345127
Start	42460620:42460620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1685C>A
AA Mutation	p.Ser562Tyr(p.S562Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000345127
Start	42464976:42464976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1058C>T
AA Mutation	p.Ser353Leu(p.S353L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345127
Start	42465161:42465161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.873T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_retained_variant
Transcription ID	ENST00000345127
Start	42459809:42459809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2496A>G
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PRICKLE1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000345127
Start	42460099:42460099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2206C>A
AA Mutation	p.His736Asn(p.H736N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000345127
Start	42464583:42464583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1451C>T
AA Mutation	p.Ala484Val(p.A484V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000345127
Start	42460548:42460548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1757C>A
AA Mutation	p.Ser586Tyr(p.S586Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000345127
Start	42466226:42466226(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.743C>T
AA Mutation	p.Ala248Val(p.A248V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000345127
Start	42468715:42468715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.499G>A
AA Mutation	p.Asp167Asn(p.D167N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000345127
Start	42459936:42459936(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2369G>T
AA Mutation	p.Arg790Ile(p.R790I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000345127
Start	42464919:42464919(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1115C>A
AA Mutation	p.Ser372Tyr(p.S372Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript