Colon Cancer: Gene >> MTA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000331320
Start	105464094:105464094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200007908
CDS Mutation	c.1139C>T
AA Mutation	p.Thr380Met(p.T380M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000331320
Start	105463241:105463241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368709921
CDS Mutation	c.1000G>A
AA Mutation	p.Asp334Asn(p.D334N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000331320
Start	105464786:105464786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1457G>A
AA Mutation	p.Cys486Tyr(p.C486Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000331320
Start	105460405:105460405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782330213
CDS Mutation	c.701G>A
AA Mutation	p.Arg234Gln(p.R234Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000331320
Start	105469967:105469967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1972T>C
AA Mutation	p.Phe658Leu(p.F658L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000331320
Start	105465150:105465150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1591C>T
AA Mutation	p.Arg531Cys(p.R531C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000331320
Start	105469481:105469481(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1828G>A
AA Mutation	p.Gly610Arg(p.G610R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000331320
Start	105460916:105460916(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.905A>G
AA Mutation	p.Lys302Arg(p.K302R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000331320
Start	105464078:105464078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139214108
CDS Mutation	c.1123G>A
AA Mutation	p.Gly375Ser(p.G375S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000331320
Start	105464466:105464466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1243C>T
AA Mutation	p.Arg415Cys(p.R415C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000331320
Start	105449400:105449400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782756415
CDS Mutation	c.232G>A
AA Mutation	p.Gly78Ser(p.G78S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331320
Start	105466523:105466523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141109138
CDS Mutation	c.1722C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331320
Start	105464101:105464101(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs587670754
CDS Mutation	c.1146G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331320
Start	105460860:105460860(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782204369
CDS Mutation	c.849C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331320
Start	105438676:105438676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148162904
CDS Mutation	c.33C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331320
Start	105460427:105460427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199606459
CDS Mutation	c.723C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331320
Start	105460899:105460899(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146792849
CDS Mutation	c.888C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000331320
Start	105466433:105466433(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1636delC
AA Mutation	p.Arg546AlafsTer8(p.R546Afs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000331320
Start	105466528:105466528(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1731delC
AA Mutation	p.Thr578ProfsTer18(p.T578Pfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> MTA1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331320
Start	105464089:105464089(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148214371
CDS Mutation	c.1134C>T
Mutation Classification	Silent
Feature Type	Transcript