Colon Cancer: Gene >> DIS3L2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000325385
Start	232300107:232300107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200386096
CDS Mutation	c.1727G>A
AA Mutation	p.Arg576His(p.R576H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000325385
Start	232334722:232334722(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368280072
CDS Mutation	c.2381G>A
AA Mutation	p.Arg794His(p.R794H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000325385
Start	232136590:232136590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.821G>A
AA Mutation	p.Arg274Gln(p.R274Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000325385
Start	232136698:232136698(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.929A>G
AA Mutation	p.Glu310Gly(p.E310G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000325385
Start	232334691:232334691(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754474723
CDS Mutation	c.2350G>A
AA Mutation	p.Val784Met(p.V784M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000325385
Start	232238565:232238565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1237G>A
AA Mutation	p.Val413Met(p.V413M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000325385
Start	232330763:232330763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1997C>T
AA Mutation	p.Ser666Phe(p.S666F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000325385
Start	232087581:232087581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.461C>T
AA Mutation	p.Ser154Phe(p.S154F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000325385
Start	232333943:232333943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2114G>A
AA Mutation	p.Arg705His(p.R705H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000325385
Start	232335854:232335854(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201189209
CDS Mutation	c.2476G>A
AA Mutation	p.Glu826Lys(p.E826K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325385
Start	232263422:232263422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762905765
CDS Mutation	c.1641C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325385
Start	232335820:232335820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2442G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325385
Start	232087639:232087639(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143680532
CDS Mutation	c.519C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000325385
Start	232263321:232263321(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1545delC
AA Mutation	p.Ile516PhefsTer15(p.I516Ffs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000325385
Start	232329903:232329903(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1835delC
AA Mutation	p.Pro612ArgfsTer33(p.P612Rfs*33)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000325385
Start	232130690:232130690(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.673delT
AA Mutation	p.Ser225ArgfsTer113(p.S225Rfs*113)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000325385
Start	232130692:232130693(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.675_676delGG
AA Mutation	p.Lys227IlefsTer29(p.K227Ifs*29)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000325385
Start	232334638:232334639(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2302dupC
AA Mutation	p.Leu768ProfsTer56(p.L768Pfs*56)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000325385
Start	232163543:232163544(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1035_1036insAAAAGTAAA
AA Mutation	p.Ser345_Asp346insLysSerLys(p.S345_D346insKSK)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> DIS3L2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000325385
Start	232333940:232333940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2111G>A
AA Mutation	p.Arg704His(p.R704H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000325385
Start	232030019:232030019(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372013568
CDS Mutation	c.305G>A
AA Mutation	p.Arg102His(p.R102H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000325385
Start	232087501:232087501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.381G>T
AA Mutation	p.Glu127Asp(p.E127D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000325385
Start	232136688:232136688(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.919G>T
AA Mutation	p.Asp307Tyr(p.D307Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript