Colon Cancer: Gene >> PROX1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261454
Start	213997218:213997218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.683G>A
AA Mutation	p.Arg228Gln(p.R228Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261454
Start	213996557:213996557(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.22G>A
AA Mutation	p.Ala8Thr(p.A8T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261454
Start	214011663:214011663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1976G>T
AA Mutation	p.Cys659Phe(p.C659F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261454
Start	213997757:213997757(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1222C>T
AA Mutation	p.Arg408Cys(p.R408C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261454
Start	214035746:214035746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2126C>T
AA Mutation	p.Ala709Val(p.A709V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000261454
Start	213997160:213997160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.625C>T
AA Mutation	p.Arg209Cys(p.R209C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000261454
Start	213998006:213998006(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1471T>C
AA Mutation	p.Tyr491His(p.Y491H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000261454
Start	213997374:213997374(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs112763420
CDS Mutation	c.839G>A
AA Mutation	p.Arg280His(p.R280H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000261454
Start	213997758:213997758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776561749
CDS Mutation	c.1223G>A
AA Mutation	p.Arg408His(p.R408H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000261454
Start	214005228:214005228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1789T>C
AA Mutation	p.Tyr597His(p.Y597H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000261454
Start	213997332:213997332(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.797C>T
AA Mutation	p.Ser266Leu(p.S266L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000261454
Start	213997464:213997464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.929G>A
AA Mutation	p.Arg310Gln(p.R310Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261454
Start	213998212:213998212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755137171
CDS Mutation	c.1677C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261454
Start	213997486:213997486(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.951G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261454
Start	214005200:214005200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1761A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261454
Start	213998173:213998173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1638C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261454
Start	213996793:213996793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.258T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261454
Start	213997411:213997411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779626865
CDS Mutation	c.876C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261454
Start	214005194:214005194(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1755G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261454
Start	213996656:213996656(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.126delT
AA Mutation	p.Phe42LeufsTer4(p.F42Lfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261454
Start	213996943:213996943(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.413delC
AA Mutation	p.Pro138GlnfsTer12(p.P138Qfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PROX1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261454
Start	213997390:213997390(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.855T>G
AA Mutation	p.Asp285Glu(p.D285E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261454
Start	214005267:214005267(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745534059
CDS Mutation	c.1828G>A
AA Mutation	p.Val610Ile(p.V610I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261454
Start	213997055:213997055(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.520C>T
AA Mutation	p.Arg174Trp(p.R174W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261454
Start	214005213:214005213(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1780delT
AA Mutation	p.Tyr594IlefsTer10(p.Y594Ifs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript