Colon Cancer: Gene >> SV2A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369146
Start	149908168:149908168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1418G>A
AA Mutation	p.Arg473His(p.R473H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369146
Start	149909495:149909495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782353989
CDS Mutation	c.1256G>A
AA Mutation	p.Arg419His(p.R419H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369146
Start	149911874:149911874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.729C>A
AA Mutation	p.Ser243Arg(p.S243R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000369146
Start	149906028:149906028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764888560
CDS Mutation	c.1897G>A
AA Mutation	p.Val633Met(p.V633M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000369146
Start	149910868:149910868(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781948463
CDS Mutation	c.913G>A
AA Mutation	p.Val305Met(p.V305M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000369146
Start	149913804:149913804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781957523
CDS Mutation	c.37C>T
AA Mutation	p.Arg13Cys(p.R13C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000369146
Start	149905985:149905985(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1940G>A
AA Mutation	p.Ser647Asn(p.S647N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000369146
Start	149910583:149910583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1076G>A
AA Mutation	p.Arg359His(p.R359H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000369146
Start	149913303:149913303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782745503
CDS Mutation	c.538G>A
AA Mutation	p.Gly180Ser(p.G180S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000369146
Start	149913407:149913407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.434G>A
AA Mutation	p.Arg145Gln(p.R145Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000369146
Start	149913416:149913416(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782157459
CDS Mutation	c.425G>A
AA Mutation	p.Arg142Gln(p.R142Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000369146
Start	149913371:149913371(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781926005
CDS Mutation	c.470G>A
AA Mutation	p.Arg157Gln(p.R157Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000369146
Start	149913375:149913375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.466C>A
AA Mutation	p.Leu156Ile(p.L156I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000369146
Start	149911836:149911836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.767G>A
AA Mutation	p.Gly256Asp(p.G256D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369146
Start	149906029:149906029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782654866
CDS Mutation	c.1896C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369146
Start	149911931:149911931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.672T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369146
Start	149908113:149908113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782094239
CDS Mutation	c.1473C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369146
Start	149913429:149913429(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.412delG
AA Mutation	p.Glu138ArgfsTer39(p.E138Rfs*39)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000369146
Start	149909812:149909812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782478152
CDS Mutation	c.1168C>T
AA Mutation	p.Arg390Ter(p.R390*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	stop_gained
Transcription ID	ENST00000369146
Start	149913420:149913420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147086816
CDS Mutation	c.421C>T
AA Mutation	p.Arg141Ter(p.R141*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369146
Start	149913428:149913429(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.412dupG
AA Mutation	p.Glu138GlyfsTer16(p.E138Gfs*16)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369146
Start	149913466:149913467(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.374dupG
AA Mutation	p.Ser127GlufsTer2(p.S127Efs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> SV2A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369146
Start	149913317:149913317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.524C>A
AA Mutation	p.Ala175Glu(p.A175E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369146
Start	149913511:149913511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.330C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369146
Start	149913429:149913429(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.412delG
AA Mutation	p.Glu138ArgfsTer39(p.E138Rfs*39)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript