Colon Cancer: Gene >> RALY

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000246194
Start	34075900:34075900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.404C>T
AA Mutation	p.Ser135Leu(p.S135L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000246194
Start	34072178:34072178(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.104A>C
AA Mutation	p.Lys35Thr(p.K35T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000246194
Start	34072307:34072307(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.233G>A
AA Mutation	p.Arg78Gln(p.R78Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000246194
Start	34076791:34076791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746684649
CDS Mutation	c.634G>A
AA Mutation	p.Ala212Thr(p.A212T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000246194
Start	34077110:34077110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375332496
CDS Mutation	c.741C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000246194
Start	34075979:34075979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141301283
CDS Mutation	c.483C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000246194
Start	34077233:34077233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374165525
CDS Mutation	c.864C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000246194
Start	34072226:34072246(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.152_172delGTTCTGTGCACAAGGGCTATG
AA Mutation	p.Cys51_Ala58delinsSer(p.C51_A58delinsS)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> RALY

Mutation ID	1
Mutation Consequence	stop_gained
Transcription ID	ENST00000246194
Start	34077177:34077177(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.808C>T
AA Mutation	p.Gln270Ter(p.Q270*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript