Colon Cancer: Gene >> ITGA9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264741
Start	37777486:37777486(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2636C>T
AA Mutation	p.Ala879Val(p.A879V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264741
Start	37818966:37818966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3085G>A
AA Mutation	p.Asp1029Asn(p.D1029N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264741
Start	37519302:37519302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147821910
CDS Mutation	c.1184C>T
AA Mutation	p.Ala395Val(p.A395V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000264741
Start	37785007:37785007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs564392934
CDS Mutation	c.2818C>T
AA Mutation	p.Arg940Cys(p.R940C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000264741
Start	37494513:37494513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.557A>C
AA Mutation	p.Lys186Thr(p.K186T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000264741
Start	37653735:37653735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757894032
CDS Mutation	c.1861C>T
AA Mutation	p.Arg621Cys(p.R621C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000264741
Start	37471132:37471132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775282230
CDS Mutation	c.311G>A
AA Mutation	p.Arg104Gln(p.R104Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000264741
Start	37526058:37526058(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199626430
CDS Mutation	c.1360G>A
AA Mutation	p.Val454Met(p.V454M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000264741
Start	37513815:37513815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.950G>A
AA Mutation	p.Gly317Asp(p.G317D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264741
Start	37508579:37508579(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.849C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264741
Start	37803864:37803864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761430711
CDS Mutation	c.2931C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264741
Start	37513813:37513813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs137951340
CDS Mutation	c.948C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000264741
Start	37452477:37452477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.103C>T
AA Mutation	p.Gln35Ter(p.Q35*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000264741
Start	37750522:37750522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2494C>T
AA Mutation	p.Arg832Ter(p.R832*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000264741
Start	37741740:37741740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2245G>T
AA Mutation	p.Glu749Ter(p.E749*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ITGA9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264741
Start	37473377:37473377(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759719660
CDS Mutation	c.337G>A
AA Mutation	p.Gly113Arg(p.G113R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000264741
Start	37741818:37741818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369201522
CDS Mutation	c.2323G>A
AA Mutation	p.Gly775Arg(p.G775R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264741
Start	37750481:37750481(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2453G>T
AA Mutation	p.Ser818Ile(p.S818I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000264741
Start	37784984:37784984(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2795C>T
AA Mutation	p.Ser932Leu(p.S932L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000264741
Start	37471116:37471116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757214035
CDS Mutation	c.295G>A
AA Mutation	p.Glu99Lys(p.E99K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264741
Start	37471019:37471019(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747154358
CDS Mutation	c.198C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264741
Start	37777514:37777514(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2664C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000264741
Start	37523613:37523613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367550460
CDS Mutation	c.1327+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript