Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> ARHGAP30

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368013
Start	161056503:161056503(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.230A>G
AA Mutation	p.Asp77Gly(p.D77G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000368013
Start	161048670:161048670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2351A>C
AA Mutation	p.Glu784Ala(p.E784A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000368013
Start	161047810:161047810(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3211A>G
AA Mutation	p.Arg1071Gly(p.R1071G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000368013
Start	161048398:161048398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2623G>A
AA Mutation	p.Ala875Thr(p.A875T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000368013
Start	161051517:161051517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1217G>A
AA Mutation	p.Arg406His(p.R406H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000368013
Start	161048949:161048949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2072A>C
AA Mutation	p.Asp691Ala(p.D691A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000368013
Start	161052484:161052484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.896G>A
AA Mutation	p.Gly299Asp(p.G299D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000368013
Start	161059650:161059650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757669760
CDS Mutation	c.164G>A
AA Mutation	p.Arg55His(p.R55H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000368013
Start	161047879:161047879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3142A>G
AA Mutation	p.Ser1048Gly(p.S1048G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000368013
Start	161048764:161048764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2257G>A
AA Mutation	p.Glu753Lys(p.E753K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000368013
Start	161047833:161047833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200017624
CDS Mutation	c.3188G>A
AA Mutation	p.Arg1063Gln(p.R1063Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000368013
Start	161052770:161052770(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200926712
CDS Mutation	c.692C>T
AA Mutation	p.Ser231Leu(p.S231L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000368013
Start	161052786:161052786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.676G>A
AA Mutation	p.Glu226Lys(p.E226K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000368013
Start	161056408:161056408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773484463
CDS Mutation	c.325C>T
AA Mutation	p.Arg109Trp(p.R109W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000368013
Start	161052320:161052320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.984G>A
AA Mutation	p.Met328Ile(p.M328I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000368013
Start	161054469:161054469(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.433C>A
AA Mutation	p.Leu145Met(p.L145M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000368013
Start	161052794:161052794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.668G>A
AA Mutation	p.Gly223Asp(p.G223D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368013
Start	161047829:161047829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3192T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368013
Start	161049664:161049664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1446C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368013
Start	161048123:161048123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2898G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368013
Start	161048705:161048705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2316G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368013
Start	161049607:161049607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761754351
CDS Mutation	c.1503G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368013
Start	161048195:161048195(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2826delC
AA Mutation	p.Lys943SerfsTer61(p.K943Sfs*61)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ARHGAP30

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368013
Start	161052660:161052660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.802C>T
AA Mutation	p.Pro268Ser(p.P268S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000368013
Start	161048856:161048856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2165G>A
AA Mutation	p.Gly722Asp(p.G722D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000368013
Start	161048064:161048064(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2957G>A
AA Mutation	p.Arg986Gln(p.R986Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000368013
Start	161059669:161059669(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.145G>T
AA Mutation	p.Val49Leu(p.V49L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368013
Start	161048942:161048942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2079G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368013
Start	161048273:161048273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2748C>T
Mutation Classification	Silent
Feature Type	Transcript