Colon Cancer: Gene >> SNRK

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000296088
Start	43303292:43303292(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.89T>C
AA Mutation	p.Val30Ala(p.V30A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000296088
Start	43303784:43303784(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.581C>A
AA Mutation	p.Pro194His(p.P194H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000296088
Start	43348417:43348417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201545457
CDS Mutation	c.2158C>T
AA Mutation	p.Arg720Trp(p.R720W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000296088
Start	43347802:43347802(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1543A>G
AA Mutation	p.Asn515Asp(p.N515D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000296088
Start	43347863:43347863(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1604G>A
AA Mutation	p.Gly535Asp(p.G535D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000296088
Start	43348447:43348447(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs572465919
CDS Mutation	c.2188G>A
AA Mutation	p.Val730Met(p.V730M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000296088
Start	43347959:43347959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1700G>T
AA Mutation	p.Arg567Leu(p.R567L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000296088
Start	43348418:43348418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200514916
CDS Mutation	c.2159G>A
AA Mutation	p.Arg720Gln(p.R720Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296088
Start	43303668:43303668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749145259
CDS Mutation	c.465G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296088
Start	43303227:43303227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.24T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296088
Start	43347933:43347933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs55661592
CDS Mutation	c.1674C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000296088
Start	43303634:43303635(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.431_432delAT
AA Mutation	p.Asn144SerfsTer5(p.N144Sfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000296088
Start	43340483:43340483(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.928C>T
AA Mutation	p.Arg310Ter(p.R310*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000296088
Start	43303548:43303549(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.345_346insTCAATAACTTTTACT
AA Mutation	p.Leu115_Ala116insSerIleThrPheThr(p.L115_A116insSITFT)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> SNRK

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000296088
Start	43303694:43303694(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.491A>C
AA Mutation	p.Lys164Thr(p.K164T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000296088
Start	43343378:43343378(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.979G>A
AA Mutation	p.Ala327Thr(p.A327T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000296088
Start	43347913:43347913(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1654C>T
AA Mutation	p.Arg552Trp(p.R552W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000296088
Start	43340312:43340312(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.757G>T
AA Mutation	p.Asp253Tyr(p.D253Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000296088
Start	43303354:43303354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.151A>C
AA Mutation	p.Lys51Gln(p.K51Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript