Colon Cancer: Gene >> PAX1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000398485
Start	21706854:21706854(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.703G>A
AA Mutation	p.Glu235Lys(p.E235K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000398485
Start	21709291:21709291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143731938
CDS Mutation	c.1129G>A
AA Mutation	p.Gly377Ser(p.G377S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000398485
Start	21708630:21708630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.989C>A
AA Mutation	p.Ala330Asp(p.A330D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000398485
Start	21706650:21706650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.499G>A
AA Mutation	p.Gly167Arg(p.G167R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000398485
Start	21706564:21706564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.413G>A
AA Mutation	p.Arg138Gln(p.R138Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000398485
Start	21706918:21706918(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.767A>G
AA Mutation	p.Tyr256Cys(p.Y256C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000398485
Start	21706837:21706837(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767391855
CDS Mutation	c.686C>T
AA Mutation	p.Ala229Val(p.A229V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000398485
Start	21707001:21707001(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.850C>T
AA Mutation	p.Arg284Cys(p.R284C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000398485
Start	21706935:21706935(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.784C>T
AA Mutation	p.Pro262Ser(p.P262S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000398485
Start	21706651:21706651(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.500G>A
AA Mutation	p.Gly167Glu(p.G167E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000398485
Start	21706575:21706575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.424G>A
AA Mutation	p.Val142Ile(p.V142I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398485
Start	21709302:21709302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754172263
CDS Mutation	c.1140C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398485
Start	21706583:21706583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.432C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398485
Start	21706853:21706853(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.702C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398485
Start	21706877:21706877(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.726G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398485
Start	21707042:21707042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.891C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398485
Start	21705739:21705739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.27G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000398485
Start	21707058:21707058(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.907G>T
AA Mutation	p.Glu303Ter(p.E303*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> PAX1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000398485
Start	21706981:21706981(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.830C>T
AA Mutation	p.Ala277Val(p.A277V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript