Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> RPS6KA5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000614987
Start	90947449:90947449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.496G>A
AA Mutation	p.Glu166Lys(p.E166K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000614987
Start	90902945:90902945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376247617
CDS Mutation	c.982G>A
AA Mutation	p.Ala328Thr(p.A328T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000614987
Start	91001159:91001159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.104C>A
AA Mutation	p.Ala35Asp(p.A35D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000614987
Start	90906232:90906232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.874C>A
AA Mutation	p.Arg292Ser(p.R292S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000614987
Start	90899391:90899391(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1411G>A
AA Mutation	p.Ala471Thr(p.A471T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000614987
Start	90900211:90900211(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1276G>T
AA Mutation	p.Asp426Tyr(p.D426Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000614987
Start	90947464:90947464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.481A>G
AA Mutation	p.Ile161Val(p.I161V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000614987
Start	90875317:90875317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373786141
CDS Mutation	c.1880G>A
AA Mutation	p.Arg627Gln(p.R627Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000614987
Start	90978500:90978500(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756086272
CDS Mutation	c.200G>A
AA Mutation	p.Arg67His(p.R67H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000614987
Start	90890496:90890496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765131434
CDS Mutation	c.1827C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000614987
Start	90900182:90900182(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1305T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000614987
Start	90873662:90873662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs562360365
CDS Mutation	c.2130C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000614987
Start	90872286:90872286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2197C>T
AA Mutation	p.Gln733Ter(p.Q733*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> RPS6KA5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000614987
Start	90875243:90875243(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747531260
CDS Mutation	c.1954G>T
AA Mutation	p.Ala652Ser(p.A652S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000614987
Start	90875317:90875317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373786141
CDS Mutation	c.1880G>A
AA Mutation	p.Arg627Gln(p.R627Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000614987
Start	90920226:90920226(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.786T>A
AA Mutation	p.Asn262Lys(p.N262K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000614987
Start	90947449:90947449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.496G>A
AA Mutation	p.Glu166Lys(p.E166K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000614987
Start	90943165:90943165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.531T>C
Mutation Classification	Silent
Feature Type	Transcript