Colon Cancer: Gene >> YTHDF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370339
Start	63196721:63196721(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377660170
CDS Mutation	c.1667G>A
AA Mutation	p.Arg556Gln(p.R556Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370339
Start	63202729:63202729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1211G>T
AA Mutation	p.Arg404Leu(p.R404L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000370339
Start	63213911:63213911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.85G>T
AA Mutation	p.Val29Phe(p.V29F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000370339
Start	63203719:63203719(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373868224
CDS Mutation	c.221C>T
AA Mutation	p.Pro74Leu(p.P74L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000370339
Start	63202636:63202636(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1304A>C
AA Mutation	p.Tyr435Ser(p.Y435S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370339
Start	63202935:63202935(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753193369
CDS Mutation	c.1005C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370339
Start	63203373:63203373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.567C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370339
Start	63202575:63202575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1365C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370339
Start	63202932:63202932(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs34046235
CDS Mutation	c.1008G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000370339
Start	63203476:63203476(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.464delC
AA Mutation	p.Pro155ArgfsTer26(p.P155Rfs*26)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> YTHDF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370339
Start	63203713:63203713(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.227C>A
AA Mutation	p.Ser76Tyr(p.S76Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370339
Start	63203427:63203427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147844381
CDS Mutation	c.513C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370339
Start	63203556:63203556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746455610
CDS Mutation	c.384G>A
Mutation Classification	Silent
Feature Type	Transcript