Colon Cancer: Gene >> MED15

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263205
Start	20566572:20566572(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.796G>A
AA Mutation	p.Ala266Thr(p.A266T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000263205
Start	20582611:20582611(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1273G>A
AA Mutation	p.Val425Ile(p.V425I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263205
Start	20566593:20566593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.817C>T
AA Mutation	p.Pro273Ser(p.P273S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000263205
Start	20537202:20537202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.154C>T
AA Mutation	p.Arg52Trp(p.R52W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000263205
Start	20584865:20584865(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1814C>T
AA Mutation	p.Pro605Leu(p.P605L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000263205
Start	20555098:20555098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751619080
CDS Mutation	c.401C>T
AA Mutation	p.Ser134Leu(p.S134L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000263205
Start	20584937:20584937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1886T>C
AA Mutation	p.Ile629Thr(p.I629T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000263205
Start	20566797:20566797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1021A>G
AA Mutation	p.Thr341Ala(p.T341A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000263205
Start	20551488:20551488(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.208+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000263205
Start	20564609:20564610(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs749884434
CDS Mutation	c.626_628dupAGC
AA Mutation	p.Gln209dup(p.Q209dup)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> MED15

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263205
Start	20507699:20507699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.21G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263205
Start	20566598:20566598(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201812389
CDS Mutation	c.822G>A
Mutation Classification	Silent
Feature Type	Transcript