Colon Cancer: Gene >> PYGB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000216962
Start	25294286:25294286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2306A>G
AA Mutation	p.His769Arg(p.H769R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000216962
Start	25278321:25278321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.858C>A
AA Mutation	p.Phe286Leu(p.F286L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000216962
Start	25292453:25292453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200843501
CDS Mutation	c.2017G>A
AA Mutation	p.Glu673Lys(p.E673K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000216962
Start	25259273:25259273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200651502
CDS Mutation	c.280C>T
AA Mutation	p.Arg94Cys(p.R94C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000216962
Start	25280983:25280983(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776622403
CDS Mutation	c.1274G>A
AA Mutation	p.Arg425His(p.R425H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000216962
Start	25294207:25294207(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200955420
CDS Mutation	c.2227G>A
AA Mutation	p.Val743Met(p.V743M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000216962
Start	25259274:25259274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769655708
CDS Mutation	c.281G>A
AA Mutation	p.Arg94His(p.R94H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000216962
Start	25281015:25281015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1306G>A
AA Mutation	p.Asp436Asn(p.D436N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000216962
Start	25295668:25295668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202186644
CDS Mutation	c.2377C>T
AA Mutation	p.Arg793Trp(p.R793W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000216962
Start	25259307:25259307(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.314T>C
AA Mutation	p.Leu105Pro(p.L105P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000216962
Start	25271454:25271454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.496A>G
AA Mutation	p.Ile166Val(p.I166V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000216962
Start	25278411:25278411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.948G>T
AA Mutation	p.Lys316Asn(p.K316N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000216962
Start	25279111:25279111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1054C>T
AA Mutation	p.Arg352Trp(p.R352W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000216962
Start	25292579:25292579(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201026212
CDS Mutation	c.2143C>T
AA Mutation	p.Arg715Trp(p.R715W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000216962
Start	25259306:25259306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201324493
CDS Mutation	c.313C>T
AA Mutation	p.Leu105Phe(p.L105F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000216962
Start	25292540:25292540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2104G>A
AA Mutation	p.Glu702Lys(p.E702K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000216962
Start	25281079:25281079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200462235
CDS Mutation	c.1370C>T
AA Mutation	p.Ala457Val(p.A457V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000216962
Start	25292553:25292553(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2117C>T
AA Mutation	p.Ala706Val(p.A706V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216962
Start	25295643:25295643(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767101832
CDS Mutation	c.2352C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216962
Start	25292464:25292464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2028C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216962
Start	25281098:25281098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201316067
CDS Mutation	c.1389C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216962
Start	25294266:25294266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199570469
CDS Mutation	c.2286C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216962
Start	25278414:25278414(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147846111
CDS Mutation	c.951C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216962
Start	25274603:25274603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs35481467
CDS Mutation	c.540C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000216962
Start	25292466:25292466(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2030delC
AA Mutation	p.Thr677LysfsTer4(p.T677Kfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000216962
Start	25288423:25288423(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775018186
CDS Mutation	c.1769-2A>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> PYGB

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216962
Start	25290486:25290486(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752184187
CDS Mutation	c.1833G>A
Mutation Classification	Silent
Feature Type	Transcript