Colon Cancer: Gene >> STK33

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000315204
Start	8454808:8454808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.722T>G
AA Mutation	p.Leu241Arg(p.L241R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000315204
Start	8392566:8392566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1489G>A
AA Mutation	p.Ala497Thr(p.A497T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000315204
Start	8457370:8457370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.668C>T
AA Mutation	p.Ala223Val(p.A223V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000315204
Start	8474730:8474730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.176G>T
AA Mutation	p.Arg59Ile(p.R59I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000315204
Start	8474765:8474765(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.141C>A
AA Mutation	p.Ser47Arg(p.S47R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000315204
Start	8436135:8436135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs550787324
CDS Mutation	c.952C>T
AA Mutation	p.Arg318Cys(p.R318C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315204
Start	8392591:8392591(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1464C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315204
Start	8452886:8452886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs557756682
CDS Mutation	c.807G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315204
Start	8413675:8413675(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779391532
CDS Mutation	c.1164G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315204
Start	8436091:8436091(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.996T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315204
Start	8440695:8440695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs531828477
CDS Mutation	c.930C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000315204
Start	8474715:8474715(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.191delA
AA Mutation	p.Asn64IlefsTer6(p.N64Ifs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000315204
Start	8464724:8464724(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.438delA
AA Mutation	p.Val147Ter(p.V147*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000315204
Start	8457443:8457443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.595G>T
AA Mutation	p.Glu199Ter(p.E199*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> STK33

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000315204
Start	8457464:8457464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.574A>G
AA Mutation	p.Met192Val(p.M192V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000315204
Start	8440691:8440691(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.934G>A
AA Mutation	p.Val312Ile(p.V312I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000315204
Start	8413648:8413648(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1191G>T
AA Mutation	p.Met397Ile(p.M397I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315204
Start	8436085:8436085(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1002A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000315204
Start	8474723:8474723(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.183delA
AA Mutation	p.Glu62LysfsTer8(p.E62Kfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript