Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> ADAM29

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359240
Start	174977590:174977590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2065A>G
AA Mutation	p.Ile689Val(p.I689V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359240
Start	174975674:174975674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.149G>T
AA Mutation	p.Gly50Val(p.G50V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000359240
Start	174975994:174975994(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.469A>G
AA Mutation	p.Lys157Glu(p.K157E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000359240
Start	174976705:174976705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1180A>C
AA Mutation	p.Ile394Leu(p.I394L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000359240
Start	174976129:174976129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.604A>G
AA Mutation	p.Ile202Val(p.I202V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000359240
Start	174977612:174977612(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748743733
CDS Mutation	c.2087G>A
AA Mutation	p.Arg696Gln(p.R696Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000359240
Start	174976457:174976457(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753780341
CDS Mutation	c.932G>A
AA Mutation	p.Arg311His(p.R311H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000359240
Start	174977114:174977114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148692882
CDS Mutation	c.1589G>A
AA Mutation	p.Arg530His(p.R530H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000359240
Start	174976723:174976723(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1198T>A
AA Mutation	p.Cys400Ser(p.C400S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000359240
Start	174976018:174976018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs555477715
CDS Mutation	c.493G>A
AA Mutation	p.Gly165Arg(p.G165R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000359240
Start	174976733:174976733(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150047888
CDS Mutation	c.1208G>A
AA Mutation	p.Gly403Asp(p.G403D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000359240
Start	174977836:174977836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373683270
CDS Mutation	c.2311C>T
AA Mutation	p.Arg771Trp(p.R771W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000359240
Start	174976832:174976832(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1307C>A
AA Mutation	p.Thr436Asn(p.T436N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000359240
Start	174975948:174975948(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.423T>G
AA Mutation	p.Phe141Leu(p.F141L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000359240
Start	174976720:174976720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746641739
CDS Mutation	c.1195C>T
AA Mutation	p.Arg399Cys(p.R399C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000359240
Start	174975978:174975978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.453G>T
AA Mutation	p.Lys151Asn(p.K151N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359240
Start	174977298:174977298(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1773G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359240
Start	174976323:174976323(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.798G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359240
Start	174977358:174977358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1833C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359240
Start	174976410:174976410(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147143176
CDS Mutation	c.885A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359240
Start	174977841:174977841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2316G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359240
Start	174975691:174975691(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.166C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359240
Start	174976800:174976800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1275T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359240
Start	174975804:174975804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.279G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359240
Start	174977283:174977283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1758C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	stop_gained
Transcription ID	ENST00000359240
Start	174976060:174976060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.535G>T
AA Mutation	p.Glu179Ter(p.E179*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359240
Start	174976240:174976241(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.717dupT
AA Mutation	p.Gly240TrpfsTer3(p.G240Wfs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359240
Start	174977619:174977620(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2101dupA
AA Mutation	p.Ser701LysfsTer2(p.S701Kfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ADAM29

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359240
Start	174977612:174977612(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748743733
CDS Mutation	c.2087G>A
AA Mutation	p.Arg696Gln(p.R696Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359240
Start	174977026:174977026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748303748
CDS Mutation	c.1501C>T
AA Mutation	p.Arg501Cys(p.R501C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000359240
Start	174975821:174975821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.296A>G
AA Mutation	p.Asn99Ser(p.N99S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript