Colon Cancer: Gene >> PSMD14

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000409682
Start	161385512:161385512(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.511G>C
AA Mutation	p.Gly171Arg(p.G171R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000409682
Start	161367862:161367862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.199G>A
AA Mutation	p.Val67Ile(p.V67I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000409682
Start	161385537:161385537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.536C>T
AA Mutation	p.Ser179Leu(p.S179L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000409682
Start	161411302:161411302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.835G>A
AA Mutation	p.Asp279Asn(p.D279N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> PSMD14

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000409682
Start	161411312:161411312(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756139595
CDS Mutation	c.845G>A
AA Mutation	p.Arg282His(p.R282H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000409682
Start	161391148:161391148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.615T>G
AA Mutation	p.Ile205Met(p.I205M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript