Colon Cancer: Gene >> TEAD3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000338863
Start	35475397:35475397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1133T>C
AA Mutation	p.Leu378Pro(p.L378P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000338863
Start	35486538:35486538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.125G>A
AA Mutation	p.Ser42Asn(p.S42N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000338863
Start	35480335:35480335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.307C>T
AA Mutation	p.Arg103Trp(p.R103W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000338863
Start	35478436:35478436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.478C>T
AA Mutation	p.Arg160Trp(p.R160W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338863
Start	35475149:35475149(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749509853
CDS Mutation	c.1203G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000338863
Start	35476343:35476343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.685G>T
AA Mutation	p.Glu229Ter(p.E229*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000338863
Start	35476436:35476436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.593-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> TEAD3

No Mutation Annotation!