Colon Cancer: Gene >> MAMLD1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262858
Start	150445535:150445535(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.19C>T
AA Mutation	p.Arg7Trp(p.R7W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262858
Start	150470178:150470178(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146555522
CDS Mutation	c.605C>T
AA Mutation	p.Thr202Met(p.T202M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262858
Start	150470700:150470700(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377084992
CDS Mutation	c.1127C>T
AA Mutation	p.Ser376Leu(p.S376L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262858
Start	150503512:150503512(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2279C>T
AA Mutation	p.Ala760Val(p.A760V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262858
Start	150470766:150470766(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1193C>T
AA Mutation	p.Ala398Val(p.A398V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000262858
Start	150445534:150445534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.18T>A
AA Mutation	p.Ser6Arg(p.S6R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000262858
Start	150470078:150470078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781882571
CDS Mutation	c.505G>A
AA Mutation	p.Val169Met(p.V169M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000262858
Start	150471300:150471300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782062169
CDS Mutation	c.1727C>T
AA Mutation	p.Pro576Leu(p.P576L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000262858
Start	150509994:150509994(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2317G>T
AA Mutation	p.Asp773Tyr(p.D773Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000262858
Start	150469828:150469828(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.255G>T
AA Mutation	p.Arg85Ser(p.R85S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000262858
Start	150471281:150471281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1708C>T
AA Mutation	p.Leu570Phe(p.L570F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000262858
Start	150503385:150503385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2152A>G
AA Mutation	p.Ser718Gly(p.S718G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000262858
Start	150470394:150470394(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.821C>T
AA Mutation	p.Pro274Leu(p.P274L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000262858
Start	150469968:150469968(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.395A>G
AA Mutation	p.Glu132Gly(p.E132G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262858
Start	150471229:150471229(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1656G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262858
Start	150469802:150469802(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.233delG
AA Mutation	p.Gly78AlafsTer36(p.G78Afs*36)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262858
Start	150503315:150503315(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2086delC
AA Mutation	p.Gln696ArgfsTer451(p.Q696Rfs*451)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000262858
Start	150470423:150470423(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.850C>T
AA Mutation	p.Gln284Ter(p.Q284*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262858
Start	150469801:150469802(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.233dupG
AA Mutation	p.Tyr79LeufsTer3(p.Y79Lfs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> MAMLD1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262858
Start	150471486:150471486(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1913G>C
AA Mutation	p.Arg638Thr(p.R638T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262858
Start	150470623:150470623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782680929
CDS Mutation	c.1050G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262858
Start	150471310:150471310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781895653
CDS Mutation	c.1737G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000262858
Start	150469834:150469834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.261C>A
AA Mutation	p.Cys87Ter(p.C87*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript