Colon Cancer: Gene >> RELT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000064780
Start	73394591:73394591(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.903G>T
AA Mutation	p.Lys301Asn(p.K301N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000064780
Start	73395115:73395115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1075C>T
AA Mutation	p.Arg359Trp(p.R359W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000064780
Start	73390810:73390810(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.176C>T
AA Mutation	p.Ala59Val(p.A59V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000064780
Start	73394237:73394237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.708G>T
AA Mutation	p.Glu236Asp(p.E236D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000064780
Start	73392347:73392347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs552980658
CDS Mutation	c.504C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000064780
Start	73394495:73394495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367815162
CDS Mutation	c.807G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000064780
Start	73395204:73395204(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1169delC
AA Mutation	p.Pro390LeufsTer7(p.P390Lfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000064780
Start	73391158:73391158(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.307delG
AA Mutation	p.Val103PhefsTer128(p.V103Ffs*128)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> RELT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000064780
Start	73395116:73395116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764847336
CDS Mutation	c.1076G>A
AA Mutation	p.Arg359Gln(p.R359Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript