Colon Cancer: Gene >> CRNKL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377340
Start	20042477:20042477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs577483196
CDS Mutation	c.1495C>T
AA Mutation	p.Arg499Cys(p.R499C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000377340
Start	20047767:20047767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1103G>A
AA Mutation	p.Arg368Gln(p.R368Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000377340
Start	20052296:20052296(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756134981
CDS Mutation	c.530C>T
AA Mutation	p.Ala177Val(p.A177V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000377340
Start	20037552:20037552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2150A>G
AA Mutation	p.Gln717Arg(p.Q717R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000377340
Start	20039742:20039742(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764813236
CDS Mutation	c.1895T>C
AA Mutation	p.Phe632Ser(p.F632S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000377340
Start	20048496:20048496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752211557
CDS Mutation	c.785G>A
AA Mutation	p.Arg262Gln(p.R262Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000377340
Start	20039609:20039609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2028G>T
AA Mutation	p.Glu676Asp(p.E676D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000377340
Start	20039626:20039626(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2011C>T
AA Mutation	p.Arg671Cys(p.R671C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377340
Start	20036327:20036327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2415C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377340
Start	20043507:20043507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771053785
CDS Mutation	c.1440C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377340
Start	20042460:20042460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752407308
CDS Mutation	c.1512C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377340
Start	20049375:20049375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750286361
CDS Mutation	c.744C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377340
Start	20052541:20052541(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.285C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000377340
Start	20037427:20037427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780569934
CDS Mutation	c.2275C>T
AA Mutation	p.Arg759Ter(p.R759*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000377340
Start	20042490:20042490(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1482G>A
AA Mutation	p.Trp494Ter(p.W494*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CRNKL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377340
Start	20049409:20049409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.710A>G
AA Mutation	p.Lys237Arg(p.K237R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377340
Start	20036313:20036313(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2429C>T
AA Mutation	p.Ala810Val(p.A810V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000377340
Start	20037474:20037474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375673644
CDS Mutation	c.2228G>A
AA Mutation	p.Arg743Gln(p.R743Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000377340
Start	20037475:20037475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2227C>T
AA Mutation	p.Arg743Ter(p.R743*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript