Colon Cancer: Gene >> STK3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000419617
Start	98596102:98596102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.752T>C
AA Mutation	p.Phe251Ser(p.F251S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000419617
Start	98767319:98767319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.160G>A
AA Mutation	p.Ala54Thr(p.A54T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000419617
Start	98455903:98455903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1415C>T
AA Mutation	p.Ala472Val(p.A472V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000419617
Start	98548106:98548106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762767274
CDS Mutation	c.1004G>A
AA Mutation	p.Gly335Asp(p.G335D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000419617
Start	98706588:98706588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.563T>C
AA Mutation	p.Met188Thr(p.M188T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000419617
Start	98749286:98749286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.341G>A
AA Mutation	p.Arg114Gln(p.R114Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000419617
Start	98579706:98579706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.906T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000419617
Start	98455993:98455993(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1325delA
AA Mutation	p.Asn442IlefsTer2(p.N442Ifs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000419617
Start	98706568:98706568(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.583G>T
AA Mutation	p.Glu195Ter(p.E195*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000419617
Start	98526740:98526740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1317+2T>G
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	splice_acceptor_variant;coding_sequence_variant;intron_variant
Transcription ID	ENST00000419617
Start	98706625:98706640(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.517-6_526delTTGCAGGATACAATGG
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> STK3

No Mutation Annotation!