Colon Cancer: Gene >> NOLC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000605788
Start	102157525:102157525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139625185
CDS Mutation	c.411T>G
AA Mutation	p.Asp137Glu(p.D137E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000605788
Start	102160605:102160605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1253C>T
AA Mutation	p.Thr418Met(p.T418M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000605788
Start	102158098:102158098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.491C>A
AA Mutation	p.Ala164Asp(p.A164D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000605788
Start	102152526:102152526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.116G>T
AA Mutation	p.Gly39Val(p.G39V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000605788
Start	102159979:102159979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.943A>C
AA Mutation	p.Lys315Gln(p.K315Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000605788
Start	102161861:102161861(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs554186651
CDS Mutation	c.1877G>A
AA Mutation	p.Arg626Gln(p.R626Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000605788
Start	102160585:102160585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762093377
CDS Mutation	c.1233C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000605788
Start	102159251:102159251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.666C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000605788
Start	102162236:102162236(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746442295
CDS Mutation	c.2067C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000605788
Start	102162138:102162138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747487000
CDS Mutation	c.1969C>T
AA Mutation	p.Arg657Ter(p.R657*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000605788
Start	102160018:102160018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.982G>T
AA Mutation	p.Glu328Ter(p.E328*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000605788
Start	102159243:102159245(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.672_674delCAG
AA Mutation	p.Ser227del(p.S227del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> NOLC1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000605788
Start	102152419:102152419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs540452525
CDS Mutation	c.9C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000605788
Start	102162209:102162209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2040C>T
Mutation Classification	Silent
Feature Type	Transcript