Colon Cancer: Gene >> NHS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000380060
Start	17725608:17725608(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750950128
CDS Mutation	c.1439G>A
AA Mutation	p.Arg480His(p.R480H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000380060
Start	17687769:17687769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.593A>C
AA Mutation	p.Lys198Thr(p.K198T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000380060
Start	17728221:17728221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4052A>T
AA Mutation	p.Lys1351Ile(p.K1351I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000380060
Start	17731917:17731917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4346C>T
AA Mutation	p.Ser1449Leu(p.S1449L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000380060
Start	17726567:17726567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2398C>T
AA Mutation	p.Leu800Phe(p.L800F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000380060
Start	17726927:17726927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771048907
CDS Mutation	c.2758G>A
AA Mutation	p.Glu920Lys(p.E920K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000380060
Start	17727998:17727998(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765167409
CDS Mutation	c.3829G>A
AA Mutation	p.Glu1277Lys(p.E1277K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000380060
Start	17725925:17725925(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1756A>T
AA Mutation	p.Ile586Phe(p.I586F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000380060
Start	17687780:17687780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.604T>C
AA Mutation	p.Tyr202His(p.Y202H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000380060
Start	17727513:17727513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763238998
CDS Mutation	c.3344C>T
AA Mutation	p.Thr1115Met(p.T1115M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000380060
Start	17721460:17721460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.872A>G
AA Mutation	p.Glu291Gly(p.E291G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000380060
Start	17727986:17727986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3817C>T
AA Mutation	p.Pro1273Ser(p.P1273S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000380060
Start	17732028:17732028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4457C>T
AA Mutation	p.Ala1486Val(p.A1486V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000380060
Start	17732367:17732367(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4796G>A
AA Mutation	p.Arg1599Gln(p.R1599Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000380060
Start	17692356:17692356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758435083
CDS Mutation	c.740G>A
AA Mutation	p.Arg247His(p.R247H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000380060
Start	17727001:17727001(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2832T>G
AA Mutation	p.Asn944Lys(p.N944K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000380060
Start	17721511:17721511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.923T>A
AA Mutation	p.Ile308Asn(p.I308N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000380060
Start	17732322:17732322(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4751G>A
AA Mutation	p.Arg1584Gln(p.R1584Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000380060
Start	17728667:17728667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4178A>G
AA Mutation	p.Asp1393Gly(p.D1393G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000380060
Start	17732088:17732088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4517G>A
AA Mutation	p.Arg1506His(p.R1506H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380060
Start	17726926:17726926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2757C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380060
Start	17692408:17692408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.792A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380060
Start	17727820:17727820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3651T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380060
Start	17727652:17727652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3483G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380060
Start	17727997:17727997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761463158
CDS Mutation	c.3828C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380060
Start	17726035:17726035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143564715
CDS Mutation	c.1866G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380060
Start	17731939:17731939(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4368C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000380060
Start	17727096:17727096(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2930delC
AA Mutation	p.Pro977HisfsTer71(p.P977Hfs*71)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000380060
Start	17692377:17692377(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.766delC
AA Mutation	p.Leu256PhefsTer28(p.L256Ffs*28)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	stop_gained
Transcription ID	ENST00000380060
Start	17724424:17724424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1171G>T
AA Mutation	p.Glu391Ter(p.E391*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	stop_gained
Transcription ID	ENST00000380060
Start	17725862:17725862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1693C>T
AA Mutation	p.Arg565Ter(p.R565*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> NHS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000380060
Start	17732438:17732438(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4867G>T
AA Mutation	p.Asp1623Tyr(p.D1623Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380060
Start	17376192:17376192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.435C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380060
Start	17725912:17725912(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148872135
CDS Mutation	c.1743G>A
Mutation Classification	Silent
Feature Type	Transcript