Colon Cancer: Gene >> ARID1B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000350026
Start	157206860:157206860(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5680A>G
AA Mutation	p.Ile1894Val(p.I1894V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000350026
Start	157201077:157201077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4444C>T
AA Mutation	p.Arg1482Cys(p.R1482C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000350026
Start	157206668:157206668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5488C>T
AA Mutation	p.Arg1830Cys(p.R1830C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000350026
Start	157201290:157201290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774777278
CDS Mutation	c.4657C>T
AA Mutation	p.Arg1553Cys(p.R1553C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000350026
Start	157206999:157206999(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5819G>A
AA Mutation	p.Arg1940His(p.R1940H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000350026
Start	157200901:157200901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4268G>A
AA Mutation	p.Gly1423Glu(p.G1423E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000350026
Start	157207775:157207775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371461578
CDS Mutation	c.6595C>T
AA Mutation	p.Arg2199Cys(p.R2199C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000350026
Start	157206448:157206448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5268C>G
AA Mutation	p.Asp1756Glu(p.D1756E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000350026
Start	157206608:157206608(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5428G>T
AA Mutation	p.Gly1810Trp(p.G1810W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000350026
Start	157167159:157167159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750810656
CDS Mutation	c.2960C>T
AA Mutation	p.Ala987Val(p.A987V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000350026
Start	157190057:157190057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3670C>T
AA Mutation	p.His1224Tyr(p.H1224Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000350026
Start	157207424:157207424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6244A>G
AA Mutation	p.Asn2082Asp(p.N2082D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000350026
Start	157200829:157200829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781209005
CDS Mutation	c.4196C>T
AA Mutation	p.Ser1399Leu(p.S1399L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000350026
Start	157203926:157203926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4916C>T
AA Mutation	p.Thr1639Met(p.T1639M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000350026
Start	157206283:157206283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5103C>A
AA Mutation	p.Asn1701Lys(p.N1701K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000350026
Start	156901478:156901478(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1840G>A
AA Mutation	p.Ala614Thr(p.A614T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000350026
Start	156778068:156778068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.139G>A
AA Mutation	p.Ala47Thr(p.A47T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000350026
Start	157084771:157084771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774701560
CDS Mutation	c.2108C>T
AA Mutation	p.Ala703Val(p.A703V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000350026
Start	157207067:157207067(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5887G>T
AA Mutation	p.Gly1963Trp(p.G1963W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000350026
Start	157110478:157110478(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2249A>G
AA Mutation	p.Gln750Arg(p.Q750R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000350026
Start	157207115:157207115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5935C>T
AA Mutation	p.Pro1979Ser(p.P1979S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000350026
Start	156829378:156829378(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754042537
CDS Mutation	c.1694G>A
AA Mutation	p.Arg565Gln(p.R565Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350026
Start	156778832:156778832(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.903C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350026
Start	157206730:157206730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755801421
CDS Mutation	c.5550C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350026
Start	157201169:157201169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4536C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350026
Start	157207156:157207156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5976G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350026
Start	157084826:157084826(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2163C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350026
Start	157207219:157207219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6039C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350026
Start	156778028:156778028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.99G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350026
Start	157207318:157207318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776483400
CDS Mutation	c.6138G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350026
Start	157207645:157207645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377350616
CDS Mutation	c.6465G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350026
Start	157201352:157201352(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746960777
CDS Mutation	c.4719G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350026
Start	156901456:156901456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1818G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350026
Start	157206814:157206814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs562880858
CDS Mutation	c.5634C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	35
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000350026
Start	157181155:157181156(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3284_3285delAA
AA Mutation	p.Lys1095ArgfsTer9(p.K1095Rfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	36
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000350026
Start	157201056:157201056(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4427delC
AA Mutation	p.Pro1476LeufsTer5(p.P1476Lfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	37
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000350026
Start	157084826:157084826(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2165delC
AA Mutation	p.Pro722HisfsTer10(p.P722Hfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	38
Mutation Consequence	stop_gained
Transcription ID	ENST00000350026
Start	157206971:157206971(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5791C>T
AA Mutation	p.Arg1931Ter(p.R1931*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	39
Mutation Consequence	stop_gained
Transcription ID	ENST00000350026
Start	157207523:157207523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6343C>T
AA Mutation	p.Arg2115Ter(p.R2115*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	40
Mutation Consequence	stop_gained
Transcription ID	ENST00000350026
Start	156935556:156935556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1978G>T
AA Mutation	p.Glu660Ter(p.E660*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	41
Mutation Consequence	stop_gained
Transcription ID	ENST00000350026
Start	157200734:157200734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4101C>A
AA Mutation	p.Tyr1367Ter(p.Y1367*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	42
Mutation Consequence	stop_gained
Transcription ID	ENST00000350026
Start	157181048:157181048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3176G>A
AA Mutation	p.Trp1059Ter(p.W1059*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	43
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000350026
Start	156778229:156778234(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.307_312delCACCAC
AA Mutation	p.His103_His104del(p.H103_H104del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ARID1B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000350026
Start	157196304:157196304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3963T>G
AA Mutation	p.Ser1321Arg(p.S1321R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000350026
Start	157206571:157206571(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5391G>T
AA Mutation	p.Gln1797His(p.Q1797H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000350026
Start	157148743:157148743(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2632T>A
AA Mutation	p.Cys878Ser(p.C878S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000350026
Start	157207067:157207067(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5887G>A
AA Mutation	p.Gly1963Arg(p.G1963R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000350026
Start	157110487:157110487(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754080772
CDS Mutation	c.2258C>T
AA Mutation	p.Pro753Leu(p.P753L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000350026
Start	157190114:157190114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752863054
CDS Mutation	c.3727C>T
AA Mutation	p.Pro1243Ser(p.P1243S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000350026
Start	156829326:156829326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778162933
CDS Mutation	c.1642G>A
AA Mutation	p.Gly548Ser(p.G548S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350026
Start	157206289:157206289(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5109A>C
Mutation Classification	Silent
Feature Type	Transcript