Colon Cancer: Gene >> YTHDC2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000161863
Start	113548595:113548595(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749627617
CDS Mutation	c.1550G>A
AA Mutation	p.Arg517His(p.R517H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000161863
Start	113553622:113553622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758300367
CDS Mutation	c.1900G>A
AA Mutation	p.Glu634Lys(p.E634K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000161863
Start	113535664:113535664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.968G>A
AA Mutation	p.Arg323Gln(p.R323Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000161863
Start	113591167:113591167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs181938024
CDS Mutation	c.3952C>T
AA Mutation	p.Arg1318Trp(p.R1318W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000161863
Start	113591168:113591168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3953G>A
AA Mutation	p.Arg1318Gln(p.R1318Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000161863
Start	113567124:113567124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373583905
CDS Mutation	c.2875C>T
AA Mutation	p.Arg959Trp(p.R959W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000161863
Start	113525081:113525081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.379G>A
AA Mutation	p.Val127Ile(p.V127I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000161863
Start	113581468:113581468(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3406C>G
AA Mutation	p.Arg1136Gly(p.R1136G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000161863
Start	113534354:113534354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760445164
CDS Mutation	c.892C>T
AA Mutation	p.Arg298Cys(p.R298C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000161863
Start	113556095:113556095(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2177T>C
AA Mutation	p.Val726Ala(p.V726A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000161863
Start	113515275:113515275(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.191T>C
AA Mutation	p.Met64Thr(p.M64T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000161863
Start	113542449:113542449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1441G>T
AA Mutation	p.Asp481Tyr(p.D481Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000161863
Start	113565951:113565951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2774T>G
AA Mutation	p.Leu925Arg(p.L925R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000161863
Start	113565909:113565909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760660765
CDS Mutation	c.2732G>A
AA Mutation	p.Arg911Gln(p.R911Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000161863
Start	113564080:113564080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2664T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000161863
Start	113561161:113561161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763490062
CDS Mutation	c.2298G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000161863
Start	113524984:113524984(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.282G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000161863
Start	113542424:113542424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763753767
CDS Mutation	c.1416C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000161863
Start	113548988:113548988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1656G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000161863
Start	113553824:113553824(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2027delA
AA Mutation	p.Asn676ThrfsTer9(p.N676Tfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000161863
Start	113526615:113526615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.505C>T
AA Mutation	p.Arg169Ter(p.R169*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	stop_gained
Transcription ID	ENST00000161863
Start	113534369:113534369(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.907G>T
AA Mutation	p.Gly303Ter(p.G303*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	stop_gained
Transcription ID	ENST00000161863
Start	113567253:113567253(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3004C>T
AA Mutation	p.Arg1002Ter(p.R1002*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	stop_gained
Transcription ID	ENST00000161863
Start	113540994:113540994(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1237G>T
AA Mutation	p.Glu413Ter(p.E413*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	stop_gained
Transcription ID	ENST00000161863
Start	113539100:113539100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1129G>T
AA Mutation	p.Glu377Ter(p.E377*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	stop_gained
Transcription ID	ENST00000161863
Start	113539148:113539148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1177G>T
AA Mutation	p.Glu393Ter(p.E393*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	stop_gained
Transcription ID	ENST00000161863
Start	113553770:113553770(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1968C>G
AA Mutation	p.Tyr656Ter(p.Y656*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	stop_gained
Transcription ID	ENST00000161863
Start	113541012:113541012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1255G>T
AA Mutation	p.Glu419Ter(p.E419*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	stop_gained
Transcription ID	ENST00000161863
Start	113591179:113591179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3964C>T
AA Mutation	p.Arg1322Ter(p.R1322*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000161863
Start	113526787:113526787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.675+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000161863
Start	113542504:113542504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1495+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> YTHDC2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000161863
Start	113526663:113526663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.553G>A
AA Mutation	p.Glu185Lys(p.E185K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000161863
Start	113553622:113553622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758300367
CDS Mutation	c.1900G>A
AA Mutation	p.Glu634Lys(p.E634K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000161863
Start	113593348:113593348(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4258C>T
AA Mutation	p.Arg1420Cys(p.R1420C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000161863
Start	113567159:113567159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2910C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000161863
Start	113567773:113567773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765103151
CDS Mutation	c.3168G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000161863
Start	113591080:113591080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3865C>T
AA Mutation	p.Arg1289Ter(p.R1289*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript