Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> TRIM24

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000343526
Start	138584910:138584910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3112A>G
AA Mutation	p.Lys1038Glu(p.K1038E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000343526
Start	138519198:138519198(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.641G>T
AA Mutation	p.Gly214Val(p.G214V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000343526
Start	138538675:138538675(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1015C>T
AA Mutation	p.Arg339Cys(p.R339C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000343526
Start	138554775:138554775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1339C>T
AA Mutation	p.Pro447Ser(p.P447S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000343526
Start	138584902:138584902(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3104C>T
AA Mutation	p.Pro1035Leu(p.P1035L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000343526
Start	138579478:138579478(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2531G>A
AA Mutation	p.Cys844Tyr(p.C844Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000343526
Start	138567599:138567599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1649C>T
AA Mutation	p.Ala550Val(p.A550V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000343526
Start	138570864:138570864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1739C>G
AA Mutation	p.Thr580Ser(p.T580S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000343526
Start	138504301:138504301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.376C>T
AA Mutation	p.Arg126Cys(p.R126C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000343526
Start	138525293:138525293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.817C>A
AA Mutation	p.Leu273Ile(p.L273I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343526
Start	138554711:138554711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147789598
CDS Mutation	c.1275C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000343526
Start	138577493:138577493(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2161C>T
AA Mutation	p.Arg721Ter(p.R721*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000343526
Start	138519212:138519212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs112052482
CDS Mutation	c.655C>T
AA Mutation	p.Arg219Ter(p.R219*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000343526
Start	138584817:138584818(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.3025dupA
AA Mutation	p.Arg1009LysfsTer10(p.R1009Kfs*10)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> TRIM24

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000343526
Start	138581706:138581706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2728C>T
AA Mutation	p.Arg910Cys(p.R910C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000343526
Start	138515349:138515349(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.621A>T
AA Mutation	p.Glu207Asp(p.E207D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000343526
Start	138577487:138577487(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2155C>T
AA Mutation	p.Pro719Ser(p.P719S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343526
Start	138515322:138515322(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.594A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000343526
Start	138577493:138577493(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2161C>T
AA Mutation	p.Arg721Ter(p.R721*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000343526
Start	138584817:138584818(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.3025dupA
AA Mutation	p.Arg1009LysfsTer10(p.R1009Kfs*10)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000343526
Start	138579379:138579380(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2433dupA
AA Mutation	p.Pro812ThrfsTer12(p.P812Tfs*12)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript