Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> RAD21

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000297338
Start	116863135:116863135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.269G>T
AA Mutation	p.Arg90Leu(p.R90L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000297338
Start	116863135:116863135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.269G>A
AA Mutation	p.Arg90Gln(p.R90Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000297338
Start	116850760:116850760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775189650
CDS Mutation	c.1478A>G
AA Mutation	p.Gln493Arg(p.Q493R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000297338
Start	116856253:116856253(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.850G>A
AA Mutation	p.Val284Ile(p.V284I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000297338
Start	116854339:116854339(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1067C>T
AA Mutation	p.Pro356Leu(p.P356L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000297338
Start	116863163:116863163(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.241G>T
AA Mutation	p.Ala81Ser(p.A81S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000297338
Start	116863210:116863210(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773855925
CDS Mutation	c.194G>A
AA Mutation	p.Arg65Gln(p.R65Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000297338
Start	116856208:116856208(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760410855
CDS Mutation	c.895A>G
AA Mutation	p.Asn299Asp(p.N299D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000297338
Start	116851967:116851967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1451A>G
AA Mutation	p.Asp484Gly(p.D484G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000297338
Start	116852690:116852690(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1180A>G
AA Mutation	p.Thr394Ala(p.T394A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297338
Start	116852619:116852619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1251C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297338
Start	116857445:116857445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.510A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297338
Start	116857415:116857415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761693720
CDS Mutation	c.540C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000297338
Start	116856244:116856245(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.858_859insT
AA Mutation	p.Met287TyrfsTer6(p.M287Yfs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> RAD21

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000297338
Start	116847532:116847532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775266057
CDS Mutation	c.1864G>A
AA Mutation	p.Ala622Thr(p.A622T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000297338
Start	116863210:116863210(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773855925
CDS Mutation	c.194G>A
AA Mutation	p.Arg65Gln(p.R65Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000297338
Start	116854322:116854322(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1084A>T
AA Mutation	p.Met362Leu(p.M362L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000297338
Start	116852090:116852090(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1328C>T
AA Mutation	p.Pro443Leu(p.P443L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000297338
Start	116849006:116849006(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1644T>G
AA Mutation	p.Asp548Glu(p.D548E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297338
Start	116856674:116856674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs34653007
CDS Mutation	c.786C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000297338
Start	116863166:116863166(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.238G>T
AA Mutation	p.Glu80Ter(p.E80*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript