Colon Cancer: Gene >> SRPK1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373825
Start	35857328:35857328(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771188043
CDS Mutation	c.1553G>A
AA Mutation	p.Arg518His(p.R518H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373825
Start	35886736:35886736(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.466G>A
AA Mutation	p.Val156Ile(p.V156I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000373825
Start	35870315:35870315(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.957G>T
AA Mutation	p.Glu319Asp(p.E319D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000373825
Start	35888815:35888815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.302A>C
AA Mutation	p.Gln101Pro(p.Q101P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000373825
Start	35835485:35835485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1787A>G
AA Mutation	p.Asp596Gly(p.D596G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000373825
Start	35886768:35886768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.434T>C
AA Mutation	p.Val145Ala(p.V145A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000373825
Start	35835339:35835339(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376455081
CDS Mutation	c.1933G>A
AA Mutation	p.Ala645Thr(p.A645T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000373825
Start	35857314:35857314(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1567C>G
AA Mutation	p.Leu523Val(p.L523V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373825
Start	35869585:35869585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1308A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373825
Start	35890899:35890899(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.189T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373825
Start	35890959:35890959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.129G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000373825
Start	35838338:35838338(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1782delA
AA Mutation	p.Gly595ValfsTer3(p.G595Vfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373825
Start	35869062:35869062(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1460delA
AA Mutation	p.Asn487MetfsTer7(p.N487Mfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373825
Start	35874244:35874244(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs34144793
CDS Mutation	c.574delA
AA Mutation	p.Ile192LeufsTer32(p.I192Lfs*32)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000373825
Start	35872722:35872722(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.592C>T
AA Mutation	p.Gln198Ter(p.Q198*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained;frameshift_variant
Transcription ID	ENST00000373825
Start	35870346:35870347(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.925_926insTCTTATAAAGATACCCC
AA Mutation	p.Ser309PhefsTer3(p.S309Ffs*3)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373825
Start	35874243:35874244(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.574dupA
AA Mutation	p.Ile192AsnfsTer10(p.I192Nfs*10)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	protein_altering_variant
Transcription ID	ENST00000373825
Start	35869568:35869569(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1324_1325insAAAACAATCATACTT
AA Mutation	p.Ile442delinsLysAsnAsnHisThrPhe(p.I442delinsKNNHTF)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> SRPK1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373825
Start	35869655:35869655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1238C>A
AA Mutation	p.Ser413Tyr(p.S413Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript