Colon Cancer: Gene >> BHLHE40

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000256495
Start	4981486:4981486(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.353T>G
AA Mutation	p.Ile118Ser(p.I118S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000256495
Start	4983558:4983558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1105G>T
AA Mutation	p.Asp369Tyr(p.D369Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000256495
Start	4983088:4983088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775412121
CDS Mutation	c.635C>T
AA Mutation	p.Ser212Leu(p.S212L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000256495
Start	4983278:4983278(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776429558
CDS Mutation	c.825C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000256495
Start	4983059:4983059(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.606G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000256495
Start	4980405:4980405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.255T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000256495
Start	4979746:4979746(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.33delC
AA Mutation	p.Ala12ProfsTer32(p.A12Pfs*32)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> BHLHE40

No Mutation Annotation!