Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> DHX32

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000284690
Start	125867087:125867087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752780900
CDS Mutation	c.379G>A
AA Mutation	p.Ala127Thr(p.A127T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000284690
Start	125852638:125852638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1097A>G
AA Mutation	p.Tyr366Cys(p.Y366C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000284690
Start	125841769:125841769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1517T>A
AA Mutation	p.Val506Glu(p.V506E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000284690
Start	125840891:125840891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1649T>G
AA Mutation	p.Ile550Ser(p.I550S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000284690
Start	125859671:125859671(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149495763
CDS Mutation	c.781C>T
AA Mutation	p.Arg261Cys(p.R261C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284690
Start	125880672:125880672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.153T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284690
Start	125880729:125880729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.96T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000284690
Start	125859797:125859798(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.654_655insAGAATCCTTTTGAG
AA Mutation	p.Pro219ArgfsTer8(p.P219Rfs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> DHX32

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000284690
Start	125839005:125839005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1877T>C
AA Mutation	p.Met626Thr(p.M626T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000284690
Start	125840981:125840981(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1559C>T
AA Mutation	p.Ser520Leu(p.S520L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284690
Start	125867022:125867022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.444C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000284690
Start	125852377:125852377(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1267G>T
AA Mutation	p.Glu423Ter(p.E423*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000284690
Start	125839120:125839120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771082972
CDS Mutation	c.1762C>T
AA Mutation	p.Arg588Ter(p.R588*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000284690
Start	125859947:125859947(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.505G>T
AA Mutation	p.Glu169Ter(p.E169*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript