Colon Cancer: Gene >> MTHFD1L

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367321
Start	151009927:151009927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs566588384
CDS Mutation	c.2234G>A
AA Mutation	p.Arg745Gln(p.R745Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367321
Start	151034499:151034499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2593A>C
AA Mutation	p.Ile865Leu(p.I865L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367321
Start	150877643:150877643(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs116360932
CDS Mutation	c.322G>A
AA Mutation	p.Asp108Asn(p.D108N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000367321
Start	150944512:150944512(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1467C>G
AA Mutation	p.Ile489Met(p.I489M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000367321
Start	150949106:150949106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139147258
CDS Mutation	c.1699G>A
AA Mutation	p.Asp567Asn(p.D567N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000367321
Start	150922235:150922235(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766519360
CDS Mutation	c.1015C>T
AA Mutation	p.Arg339Cys(p.R339C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000367321
Start	150944549:150944549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751750277
CDS Mutation	c.1504G>A
AA Mutation	p.Ala502Thr(p.A502T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000367321
Start	151036987:151036987(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2717G>A
AA Mutation	p.Cys906Tyr(p.C906Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000367321
Start	150926276:150926276(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1237A>C
AA Mutation	p.Lys413Gln(p.K413Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000367321
Start	150944555:150944555(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1510G>T
AA Mutation	p.Asp504Tyr(p.D504Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000367321
Start	150960338:150960338(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1867G>A
AA Mutation	p.Ala623Thr(p.A623T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367321
Start	150936927:150936927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371570169
CDS Mutation	c.1380G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367321
Start	151015528:151015528(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs563825223
CDS Mutation	c.2421C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367321
Start	150949123:150949123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1716G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367321
Start	150960289:150960289(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146649976
CDS Mutation	c.1818C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367321
Start	150944548:150944548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140112064
CDS Mutation	c.1503C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367321
Start	150918626:150918626(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.942G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367321
Start	150876134:150876134(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs769597461
CDS Mutation	c.278delA
AA Mutation	p.Asn93ThrfsTer18(p.N93Tfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367321
Start	150956023:150956023(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1759delA
AA Mutation	p.Ile587Ter(p.I587*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> MTHFD1L

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367321
Start	150918661:150918661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.977G>A
AA Mutation	p.Arg326Gln(p.R326Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367321
Start	150922235:150922235(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766519360
CDS Mutation	c.1015C>T
AA Mutation	p.Arg339Cys(p.R339C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367321
Start	151009856:151009856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2163G>T
AA Mutation	p.Glu721Asp(p.E721D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000367321
Start	151036977:151036977(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2707T>G
AA Mutation	p.Leu903Val(p.L903V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000367321
Start	151092518:151092518(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2899C>A
AA Mutation	p.Leu967Ile(p.L967I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript