Colon Cancer: Gene >> PXN

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000228307
Start	120224375:120224375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748821995
CDS Mutation	c.16G>A
AA Mutation	p.Ala6Thr(p.A6T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000228307
Start	120212514:120212514(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1576C>T
AA Mutation	p.His526Tyr(p.H526Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000228307
Start	120221712:120221712(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.742G>A
AA Mutation	p.Val248Ile(p.V248I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000228307
Start	120212530:120212530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1560G>T
AA Mutation	p.Gln520His(p.Q520H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000228307
Start	120214955:120214955(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1148T>C
AA Mutation	p.Val383Ala(p.V383A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000228307
Start	120214956:120214956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766354430
CDS Mutation	c.1147G>A
AA Mutation	p.Val383Ile(p.V383I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000228307
Start	120215182:120215182(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1025A>G
AA Mutation	p.Gln342Arg(p.Q342R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000228307
Start	120213974:120213974(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755276611
CDS Mutation	c.1377C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000228307
Start	120213872:120213872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772494174
CDS Mutation	c.1479G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000228307
Start	120214924:120214924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1179C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000228307
Start	120222879:120222879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374969563
CDS Mutation	c.477G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000228307
Start	120223774:120223774(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.300T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000228307
Start	120212368:120212368(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1722G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000228307
Start	120221734:120221734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.720C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000228307
Start	120215229:120215229(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.978delG
AA Mutation	p.Pro328ArgfsTer18(p.P328Rfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000228307
Start	120214891:120214891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1212C>A
AA Mutation	p.Tyr404Ter(p.Y404*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> PXN

Mutation ID	1
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000228307
Start	120222914:120222914(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.442delC
AA Mutation	p.Leu148CysfsTer5(p.L148Cfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000228307
Start	120215662:120215662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.832-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript