Colon Cancer: Gene >> ITGAM

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000287497
Start	31329270:31329270(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2835G>T
AA Mutation	p.Glu945Asp(p.E945D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000287497
Start	31330112:31330112(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369576245
CDS Mutation	c.3008G>A
AA Mutation	p.Arg1003His(p.R1003H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000287497
Start	31331249:31331249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3361G>A
AA Mutation	p.Ala1121Thr(p.A1121T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000287497
Start	31261700:31261700(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.37T>A
AA Mutation	p.Leu13Ile(p.L13I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000287497
Start	31276730:31276730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768218666
CDS Mutation	c.1069G>A
AA Mutation	p.Ala357Thr(p.A357T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000287497
Start	31271959:31271959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766435644
CDS Mutation	c.671G>A
AA Mutation	p.Arg224Gln(p.R224Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000287497
Start	31321610:31321610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368823511
CDS Mutation	c.1985G>A
AA Mutation	p.Arg662Gln(p.R662Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000287497
Start	31324745:31324745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2252T>C
AA Mutation	p.Val751Ala(p.V751A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000287497
Start	31321586:31321586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1961G>A
AA Mutation	p.Cys654Tyr(p.C654Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000287497
Start	31297916:31297916(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199951990
CDS Mutation	c.1669G>A
AA Mutation	p.Gly557Arg(p.G557R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000287497
Start	31321523:31321523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1898G>T
AA Mutation	p.Arg633Met(p.R633M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000287497
Start	31277991:31277991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755777607
CDS Mutation	c.1238G>A
AA Mutation	p.Arg413Gln(p.R413Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000287497
Start	31324706:31324706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2213T>C
AA Mutation	p.Val738Ala(p.V738A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000287497
Start	31324751:31324751(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375408663
CDS Mutation	c.2258C>T
AA Mutation	p.Ala753Val(p.A753V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287497
Start	31275620:31275620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.930T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287497
Start	31261702:31261702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.39A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287497
Start	31324984:31324984(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2316T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287497
Start	31278088:31278088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs79658154
CDS Mutation	c.1335C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287497
Start	31278028:31278028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1275A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287497
Start	31331185:31331185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3297G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287497
Start	31331266:31331266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777290963
CDS Mutation	c.3378G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287497
Start	31297921:31297921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1674C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287497
Start	31273389:31273389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372119875
CDS Mutation	c.729C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000287497
Start	31297593:31297593(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1441delC
AA Mutation	p.His481IlefsTer44(p.H481Ifs*44)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ITGAM

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000287497
Start	31330598:31330598(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3269G>A
AA Mutation	p.Arg1090Lys(p.R1090K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000287497
Start	31271918:31271918(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761171328
CDS Mutation	c.630C>A
AA Mutation	p.Asn210Lys(p.N210K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000287497
Start	31275683:31275683(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.993G>T
AA Mutation	p.Lys331Asn(p.K331N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000287497
Start	31297574:31297574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756564190
CDS Mutation	c.1417G>A
AA Mutation	p.Asp473Asn(p.D473N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287497
Start	31297588:31297588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1431C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287497
Start	31297528:31297528(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774447380
CDS Mutation	c.1371C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000287497
Start	31330371:31330371(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748170419
CDS Mutation	c.3124G>T
AA Mutation	p.Glu1042Ter(p.E1042*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript