Colon Cancer: Gene >> MAT1A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372213
Start	80283928:80283928(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.280G>T
AA Mutation	p.Asp94Tyr(p.D94Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000372213
Start	80276409:80276409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.735G>T
AA Mutation	p.Gln245His(p.Q245H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000372213
Start	80275192:80275192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138556525
CDS Mutation	c.776C>T
AA Mutation	p.Ala259Val(p.A259V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000372213
Start	80276489:80276489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.655C>T
AA Mutation	p.Arg219Cys(p.R219C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000372213
Start	80274577:80274577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370173781
CDS Mutation	c.1028G>A
AA Mutation	p.Arg343Gln(p.R343Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000372213
Start	80276513:80276513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.631G>A
AA Mutation	p.Glu211Lys(p.E211K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000372213
Start	80275138:80275138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.830A>G
AA Mutation	p.His277Arg(p.H277R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372213
Start	80275116:80275116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.852G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372213
Start	80275089:80275089(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.879A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372213
Start	80285540:80285540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.141G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000372213
Start	80273799:80273799(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1170delC
AA Mutation	p.Arg391GlyfsTer50(p.R391Gfs*50)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> MAT1A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372213
Start	80274550:80274550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1055A>G
AA Mutation	p.Asn352Ser(p.N352S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000372213
Start	80276381:80276381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.763C>T
AA Mutation	p.Pro255Ser(p.P255S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372213
Start	80276388:80276388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752764990
CDS Mutation	c.756C>T
Mutation Classification	Silent
Feature Type	Transcript