Colon Cancer: Gene >> MTHFD1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000216605
Start	64388460:64388460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.33G>T
AA Mutation	p.Glu11Asp(p.E11D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000216605
Start	64427429:64427429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1220C>T
AA Mutation	p.Ala407Val(p.A407V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000216605
Start	64431593:64431593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1373C>T
AA Mutation	p.Ala458Val(p.A458V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000216605
Start	64454822:64454822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2665C>T
AA Mutation	p.Arg889Cys(p.R889C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000216605
Start	64441453:64441453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1884G>T
AA Mutation	p.Glu628Asp(p.E628D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000216605
Start	64442096:64442096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765252643
CDS Mutation	c.1927G>A
AA Mutation	p.Ala643Thr(p.A643T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000216605
Start	64415485:64415485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.368A>G
AA Mutation	p.Asp123Gly(p.D123G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000216605
Start	64440238:64440238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1787A>C
AA Mutation	p.Lys596Thr(p.K596T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000216605
Start	64431595:64431595(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1375G>A
AA Mutation	p.Ala459Thr(p.A459T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216605
Start	64440146:64440146(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1695G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216605
Start	64440167:64440167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1716C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000216605
Start	64442303:64442304(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2043dupT
AA Mutation	p.Asn682Ter(p.N682*)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000216605
Start	64424808:64424809(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.738dupA
AA Mutation	p.Pro247ThrfsTer9(p.P247Tfs*9)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> MTHFD1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216605
Start	64453825:64453825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2529C>T
Mutation Classification	Silent
Feature Type	Transcript