Colon Cancer: Gene >> YTHDC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000344157
Start	68332812:68332812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771726851
CDS Mutation	c.1009G>A
AA Mutation	p.Val337Ile(p.V337I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000344157
Start	68333358:68333358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.923C>A
AA Mutation	p.Ser308Tyr(p.S308Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000344157
Start	68337726:68337726(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.305G>T
AA Mutation	p.Arg102Ile(p.R102I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000344157
Start	68318845:68318845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1702C>G
AA Mutation	p.Arg568Gly(p.R568G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000344157
Start	68332799:68332799(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142607687
CDS Mutation	c.1022G>A
AA Mutation	p.Arg341Gln(p.R341Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000344157
Start	68337110:68337110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.800G>A
AA Mutation	p.Arg267Gln(p.R267Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000344157
Start	68330209:68330209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1224A>T
AA Mutation	p.Lys408Asn(p.K408N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000344157
Start	68333394:68333394(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.887A>T
AA Mutation	p.Glu296Val(p.E296V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000344157
Start	68322756:68322756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1594G>A
AA Mutation	p.Val532Met(p.V532M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000344157
Start	68314214:68314214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2069C>G
AA Mutation	p.Pro690Arg(p.P690R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000344157
Start	68332809:68332809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1012C>T
AA Mutation	p.Arg338Cys(p.R338C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000344157
Start	68337122:68337122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.788A>G
AA Mutation	p.Asp263Gly(p.D263G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000344157
Start	68314277:68314277(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754708866
CDS Mutation	c.2006C>T
AA Mutation	p.Ala669Val(p.A669V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000344157
Start	68320147:68320147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1660C>T
AA Mutation	p.Pro554Ser(p.P554S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344157
Start	68337175:68337175(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757364840
CDS Mutation	c.735G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344157
Start	68316392:68316392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1881T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344157
Start	68337424:68337424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.486T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344157
Start	68322823:68322823(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1527C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000344157
Start	68314128:68314128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2155C>T
AA Mutation	p.Arg719Ter(p.R719*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000344157
Start	68318728:68318728(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1723C>T
AA Mutation	p.Arg575Ter(p.R575*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000344157
Start	68322864:68322864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1486G>T
AA Mutation	p.Glu496Ter(p.E496*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> YTHDC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000344157
Start	68349730:68349730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.24G>T
AA Mutation	p.Glu8Asp(p.E8D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000344157
Start	68337110:68337110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.800G>A
AA Mutation	p.Arg267Gln(p.R267Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000344157
Start	68338311:68338311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.102G>T
AA Mutation	p.Glu34Asp(p.E34D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000344157
Start	68337788:68337788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.243C>G
AA Mutation	p.Asn81Lys(p.N81K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344157
Start	68337175:68337175(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757364840
CDS Mutation	c.735G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000344157
Start	68337880:68337880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.151C>T
AA Mutation	p.Arg51Ter(p.R51*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript