Colon Cancer: Gene >> BEST1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000378043
Start	61951861:61951861(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765385264
CDS Mutation	c.55C>T
AA Mutation	p.Arg19Cys(p.R19C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000378043
Start	61962506:61962506(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1352A>T
AA Mutation	p.Asp451Val(p.D451V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000378043
Start	61955897:61955897(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.427G>A
AA Mutation	p.Val143Ile(p.V143I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000378043
Start	61957454:61957454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs267606679
CDS Mutation	c.704T>C
AA Mutation	p.Val235Ala(p.V235A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000378043
Start	61959989:61959989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1046C>A
AA Mutation	p.Ala349Asp(p.A349D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000378043
Start	61960040:61960040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1097T>A
AA Mutation	p.Ile366Asn(p.I366N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000378043
Start	61957403:61957403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs281865239
CDS Mutation	c.653G>A
AA Mutation	p.Arg218His(p.R218H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378043
Start	61956947:61956947(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776011957
CDS Mutation	c.585G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378043
Start	61959996:61959996(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1053C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000378043
Start	61956954:61956954(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.592G>T
AA Mutation	p.Gly198Ter(p.G198*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> BEST1

No Mutation Annotation!