Colon Cancer: Gene >> STK38

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000229812
Start	36496725:36496725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746316301
CDS Mutation	c.1253T>G
AA Mutation	p.Ile418Ser(p.I418S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000229812
Start	36498370:36498370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1069A>G
AA Mutation	p.Ile357Val(p.I357V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000229812
Start	36517774:36517774(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.457T>C
AA Mutation	p.Phe153Leu(p.F153L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000229812
Start	36506604:36506604(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.813G>C
AA Mutation	p.Trp271Cys(p.W271C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000229812
Start	36515445:36515445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.562G>A
AA Mutation	p.Glu188Lys(p.E188K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000229812
Start	36515437:36515437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.570G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000229812
Start	36540113:36540113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.90T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000229812
Start	36497806:36497806(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1146delT
AA Mutation	p.Phe382LeufsTer70(p.F382Lfs*70)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> STK38

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000229812
Start	36525636:36525636(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.138G>T
AA Mutation	p.Lys46Asn(p.K46N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000229812
Start	36525629:36525629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.145G>T
AA Mutation	p.Glu49Ter(p.E49*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript