Colon Cancer: Gene >> RGS12

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000336727
Start	3316309:3316309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200218411
CDS Mutation	c.139G>A
AA Mutation	p.Val47Ile(p.V47I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000336727
Start	3316340:3316340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.170G>C
AA Mutation	p.Gly57Ala(p.G57A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000336727
Start	3428672:3428672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760916479
CDS Mutation	c.3526A>G
AA Mutation	p.Lys1176Glu(p.K1176E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000336727
Start	3417466:3417466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758297073
CDS Mutation	c.2686G>A
AA Mutation	p.Ala896Thr(p.A896T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000336727
Start	3316856:3316856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779962906
CDS Mutation	c.686C>T
AA Mutation	p.Ala229Val(p.A229V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000336727
Start	3316859:3316859(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.689T>C
AA Mutation	p.Met230Thr(p.M230T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000336727
Start	3430767:3430767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774020891
CDS Mutation	c.3926C>T
AA Mutation	p.Ala1309Val(p.A1309V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000336727
Start	3317473:3317473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1303A>G
AA Mutation	p.Ser435Gly(p.S435G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000336727
Start	3428685:3428685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3539A>G
AA Mutation	p.Gln1180Arg(p.Q1180R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000336727
Start	3430911:3430911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200575024
CDS Mutation	c.4070C>T
AA Mutation	p.Pro1357Leu(p.P1357L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000336727
Start	3317744:3317744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1574G>A
AA Mutation	p.Gly525Asp(p.G525D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000336727
Start	3430636:3430636(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3795G>T
AA Mutation	p.Gln1265His(p.Q1265H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000336727
Start	3316477:3316477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780632548
CDS Mutation	c.307G>A
AA Mutation	p.Glu103Lys(p.E103K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000336727
Start	3417000:3417000(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769613758
CDS Mutation	c.2515C>T
AA Mutation	p.Arg839Cys(p.R839C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000336727
Start	3414078:3414078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs528303715
CDS Mutation	c.2027C>T
AA Mutation	p.Thr676Met(p.T676M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000336727
Start	3317813:3317813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1643G>A
AA Mutation	p.Cys548Tyr(p.C548Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336727
Start	3439552:3439552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs186552583
CDS Mutation	c.4212G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336727
Start	3317397:3317397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778973905
CDS Mutation	c.1227C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336727
Start	3317538:3317538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1368G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336727
Start	3317400:3317400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756319302
CDS Mutation	c.1230C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336727
Start	3425514:3425514(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375852981
CDS Mutation	c.3285C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336727
Start	3417483:3417483(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138222443
CDS Mutation	c.2703G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336727
Start	3316290:3316290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.120A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336727
Start	3316335:3316335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141866851
CDS Mutation	c.165C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336727
Start	3316275:3316275(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs184207042
CDS Mutation	c.105G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000336727
Start	3430923:3430923(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs781771156
CDS Mutation	c.4087delC
AA Mutation	p.Gln1363ArgfsTer30(p.Q1363Rfs*30)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000336727
Start	3430704:3430704(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs751982308
CDS Mutation	c.3870delC
AA Mutation	p.Gln1292ArgfsTer49(p.Q1292Rfs*49)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000336727
Start	3417086:3417086(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2606delA
AA Mutation	p.Lys869SerfsTer2(p.K869Sfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000336727
Start	3428672:3428672(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs753542639
CDS Mutation	c.3534delA
AA Mutation	p.Lys1178AsnfsTer32(p.K1178Nfs*32)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000336727
Start	3316501:3316501(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.335delG
AA Mutation	p.Gly112AspfsTer9(p.G112Dfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000336727
Start	3428126:3428127(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3369_3370delGA
AA Mutation	p.Asn1124HisfsTer23(p.N1124Hfs*23)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	stop_gained
Transcription ID	ENST00000336727
Start	3414767:3414767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2206G>T
AA Mutation	p.Glu736Ter(p.E736*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> RGS12

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336727
Start	3317127:3317127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.957G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336727
Start	3317877:3317877(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1707C>T
Mutation Classification	Silent
Feature Type	Transcript