Colon Cancer: Gene >> MALT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000348428
Start	58734365:58734365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1459G>A
AA Mutation	p.Val487Met(p.V487M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000348428
Start	58734330:58734330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1424C>A
AA Mutation	p.Pro475Gln(p.P475Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000348428
Start	58734381:58734381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769025149
CDS Mutation	c.1475C>T
AA Mutation	p.Thr492Met(p.T492M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000348428
Start	58747501:58747501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780283850
CDS Mutation	c.2134A>G
AA Mutation	p.Ile712Val(p.I712V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000348428
Start	58723203:58723203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757096789
CDS Mutation	c.1174C>T
AA Mutation	p.Arg392Cys(p.R392C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000348428
Start	58741987:58741987(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779797395
CDS Mutation	c.1726C>T
AA Mutation	p.Arg576Trp(p.R576W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000348428
Start	58747484:58747484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2117A>G
AA Mutation	p.Asn706Ser(p.N706S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000348428
Start	58709391:58709391(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374931065
CDS Mutation	c.663C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000348428
Start	58747510:58747510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2143T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000348428
Start	58710931:58710931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765314609
CDS Mutation	c.936T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000348428
Start	58681329:58681329(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.374delC
AA Mutation	p.Pro125GlnfsTer3(p.P125Qfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000348428
Start	58681300:58681300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.340G>T
AA Mutation	p.Glu114Ter(p.E114*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000348428
Start	58747522:58747522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2155C>T
AA Mutation	p.Arg719Ter(p.R719*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000348428
Start	58700550:58700550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.608G>A
AA Mutation	p.Trp203Ter(p.W203*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> MALT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000348428
Start	58709432:58709432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.704C>T
AA Mutation	p.Ser235Phe(p.S235F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000348428
Start	58696474:58696474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.485A>C
AA Mutation	p.Lys162Thr(p.K162T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000348428
Start	58741913:58741913(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1652G>A
AA Mutation	p.Arg551Gln(p.R551Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript