Colon Cancer: Gene >> RPL28

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000344063
Start	55388037:55388037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.313G>A
AA Mutation	p.Asp105Asn(p.D105N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000344063
Start	55388253:55388253(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.335G>A
AA Mutation	p.Arg112His(p.R112H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000344063
Start	55387963:55387963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.239C>A
AA Mutation	p.Thr80Asn(p.T80N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000344063
Start	55386397:55386397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.40T>C
AA Mutation	p.Ser14Pro(p.S14P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000344063
Start	55388327:55388327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.409T>C
AA Mutation	p.Ser137Pro(p.S137P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> RPL28

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000344063
Start	55388264:55388264(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745789187
CDS Mutation	c.346G>A
AA Mutation	p.Ala116Thr(p.A116T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000344063
Start	55386645:55386645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.157C>T
AA Mutation	p.Pro53Ser(p.P53S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript