Colon Cancer: Gene >> RPS6KL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000354625
Start	74907103:74907103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200816369
CDS Mutation	c.1561C>T
AA Mutation	p.Arg521Trp(p.R521W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000354625
Start	74909965:74909965(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.848C>T
AA Mutation	p.Thr283Ile(p.T283I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000354625
Start	74909821:74909821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.992G>A
AA Mutation	p.Arg331Lys(p.R331K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000354625
Start	74921441:74921441(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767222520
CDS Mutation	c.101G>A
AA Mutation	p.Arg34His(p.R34H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354625
Start	74911345:74911345(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.567G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354625
Start	74921383:74921383(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760879613
CDS Mutation	c.159G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354625
Start	74909766:74909766(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1047T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354625
Start	74909790:74909790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1023C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000354625
Start	74907048:74907048(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1616delT
AA Mutation	p.Phe539SerfsTer88(p.F539Sfs*88)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> RPS6KL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000354625
Start	74919909:74919909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746273906
CDS Mutation	c.326G>A
AA Mutation	p.Arg109Gln(p.R109Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript