Colon Cancer: Gene >> ITGA5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000293379
Start	54398664:54398664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765192718
CDS Mutation	c.2876C>T
AA Mutation	p.Ala959Val(p.A959V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000293379
Start	54405882:54405882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.951C>A
AA Mutation	p.Phe317Leu(p.F317L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000293379
Start	54405292:54405292(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1099G>T
AA Mutation	p.Val367Phe(p.V367F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000293379
Start	54398698:54398698(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377040337
CDS Mutation	c.2842C>T
AA Mutation	p.Arg948Trp(p.R948W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000293379
Start	54401624:54401624(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369973451
CDS Mutation	c.2348G>A
AA Mutation	p.Arg783Gln(p.R783Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000293379
Start	54405686:54405686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375602887
CDS Mutation	c.994G>A
AA Mutation	p.Ala332Thr(p.A332T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000293379
Start	54398619:54398619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2921A>T
AA Mutation	p.Gln974Leu(p.Q974L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000293379
Start	54419098:54419098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756815283
CDS Mutation	c.101C>T
AA Mutation	p.Pro34Leu(p.P34L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000293379
Start	54409592:54409592(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.355C>T
AA Mutation	p.Arg119Trp(p.R119W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000293379
Start	54404462:54404462(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1431G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000293379
Start	54419114:54419114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.85C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000293379
Start	54419166:54419166(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.33C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000293379
Start	54419076:54419076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.123C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000293379
Start	54409590:54409590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.357G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000293379
Start	54401379:54401379(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2487C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000293379
Start	54407655:54407655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs559129448
CDS Mutation	c.900C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000293379
Start	54405196:54405196(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1195delC
AA Mutation	p.Leu399TrpfsTer26(p.L399Wfs*26)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000293379
Start	54407655:54407658(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.897_900delTTAC
AA Mutation	p.Tyr300AlafsTer75(p.Y300Afs*75)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000293379
Start	54403660:54403660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1741C>T
AA Mutation	p.Arg581Ter(p.R581*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	stop_gained
Transcription ID	ENST00000293379
Start	54408158:54408158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.769C>T
AA Mutation	p.Gln257Ter(p.Q257*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000293379
Start	54402094:54402094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2134-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> ITGA5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000293379
Start	54404750:54404750(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1370G>A
AA Mutation	p.Gly457Asp(p.G457D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000293379
Start	54402257:54402257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2056G>A
AA Mutation	p.Gly686Ser(p.G686S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000293379
Start	54398602:54398602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2938C>T
AA Mutation	p.Arg980Cys(p.R980C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000293379
Start	54402183:54402183(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2130A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000293379
Start	54400981:54400981(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2508C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000293379
Start	54411889:54411889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.294C>A
Mutation Classification	Silent
Feature Type	Transcript