Colon Cancer: Gene >> SRGAP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000355086
Start	64142518:64142518(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3104T>C
AA Mutation	p.Met1035Thr(p.M1035T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000355086
Start	64091326:64091326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149964620
CDS Mutation	c.1487G>A
AA Mutation	p.Arg496His(p.R496H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000355086
Start	64042853:64042853(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.553G>A
AA Mutation	p.Ala185Thr(p.A185T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000355086
Start	64127677:64127677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2493G>T
AA Mutation	p.Lys831Asn(p.K831N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000355086
Start	63984061:63984061(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778174499
CDS Mutation	c.182C>T
AA Mutation	p.Thr61Met(p.T61M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000355086
Start	64126021:64126021(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749937035
CDS Mutation	c.2269C>T
AA Mutation	p.Arg757Trp(p.R757W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000355086
Start	64142418:64142418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3004C>A
AA Mutation	p.Pro1002Thr(p.P1002T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000355086
Start	64128087:64128087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200877785
CDS Mutation	c.2767C>T
AA Mutation	p.Arg923Trp(p.R923W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000355086
Start	64065215:64065215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1121A>G
AA Mutation	p.Glu374Gly(p.E374G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000355086
Start	64063089:64063089(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773806400
CDS Mutation	c.974C>T
AA Mutation	p.Ala325Val(p.A325V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000355086
Start	64128093:64128093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747622771
CDS Mutation	c.2773G>A
AA Mutation	p.Asp925Asn(p.D925N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000355086
Start	63990028:63990028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.382C>T
AA Mutation	p.Arg128Trp(p.R128W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000355086
Start	64087019:64087019(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1429A>G
AA Mutation	p.Thr477Ala(p.T477A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355086
Start	64142555:64142555(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761367082
CDS Mutation	c.3141C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355086
Start	64142432:64142432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138568906
CDS Mutation	c.3018G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355086
Start	64079017:64079017(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1224A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000355086
Start	63984041:63984041(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.168delA
AA Mutation	p.Ala57LeufsTer11(p.A57Lfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000355086
Start	64095145:64095145(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1622delT
AA Mutation	p.Phe541SerfsTer40(p.F541Sfs*40)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000355086
Start	64127883:64127883(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2567delC
AA Mutation	p.Pro856LeufsTer3(p.P856Lfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	stop_gained
Transcription ID	ENST00000355086
Start	64091331:64091331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1492C>T
AA Mutation	p.Gln498Ter(p.Q498*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000355086
Start	64042910:64042910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747219637
CDS Mutation	c.610C>T
AA Mutation	p.Arg204Ter(p.R204*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	stop_gained
Transcription ID	ENST00000355086
Start	64142487:64142487(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3073C>T
AA Mutation	p.Arg1025Ter(p.R1025*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	stop_gained
Transcription ID	ENST00000355086
Start	63983952:63983952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.73C>T
AA Mutation	p.Arg25Ter(p.R25*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	stop_gained
Transcription ID	ENST00000355086
Start	63984039:63984039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.160C>T
AA Mutation	p.Arg54Ter(p.R54*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000355086
Start	64042955:64042956(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs772889354
CDS Mutation	c.661dupA
AA Mutation	p.Met221AsnfsTer13(p.M221Nfs*13)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000355086
Start	64079104:64079105(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1311_1312insA
AA Mutation	p.Phe438IlefsTer14(p.F438Ifs*14)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> SRGAP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000355086
Start	64094974:64094974(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377564318
CDS Mutation	c.1582C>T
AA Mutation	p.Arg528Trp(p.R528W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000355086
Start	64127901:64127901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2581C>T
AA Mutation	p.Pro861Ser(p.P861S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355086
Start	63983969:63983969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.90A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355086
Start	64065123:64065123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200749162
CDS Mutation	c.1029C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000355086
Start	63989945:63989945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.299G>A
AA Mutation	p.Trp100Ter(p.W100*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript