Colon Cancer: Gene >> RPS6KB2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000312629
Start	67434467:67434467(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1138G>A
AA Mutation	p.Ala380Thr(p.A380T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000312629
Start	67434426:67434426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200633410
CDS Mutation	c.1097C>T
AA Mutation	p.Thr366Met(p.T366M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000312629
Start	67433351:67433351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767711171
CDS Mutation	c.810C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000312629
Start	67433004:67433004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377739693
CDS Mutation	c.669C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000312629
Start	67434602:67434602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768303346
CDS Mutation	c.1176G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000312629
Start	67429180:67429180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.180G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000312629
Start	67434989:67434989(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1273delC
AA Mutation	p.Leu425SerfsTer69(p.L425Sfs*69)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> RPS6KB2

No Mutation Annotation!