Colon Cancer: Gene >> ASB4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000325885
Start	95536539:95536539(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1081G>T
AA Mutation	p.Asp361Tyr(p.D361Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000325885
Start	95528238:95528238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.913G>C
AA Mutation	p.Glu305Gln(p.E305Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000325885
Start	95486137:95486137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.166G>C
AA Mutation	p.Val56Leu(p.V56L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000325885
Start	95495857:95495857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.287A>G
AA Mutation	p.Asp96Gly(p.D96G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325885
Start	95527856:95527856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.531G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325885
Start	95495978:95495978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747253499
CDS Mutation	c.408C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325885
Start	95496041:95496041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.471G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325885
Start	95527817:95527817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.492G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000325885
Start	95537581:95537582(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1108dupT
AA Mutation	p.Tyr370LeufsTer10(p.Y370Lfs*10)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ASB4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000325885
Start	95496030:95496030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.460C>A
AA Mutation	p.Leu154Ile(p.L154I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000325885
Start	95527816:95527816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138454369
CDS Mutation	c.491C>T
AA Mutation	p.Ala164Val(p.A164V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325885
Start	95486154:95486154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.183A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325885
Start	95528067:95528067(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.742C>A
Mutation Classification	Silent
Feature Type	Transcript