Colon Cancer: Gene >> SLC7A2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000494857
Start	17560390:17560390(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs549251912
CDS Mutation	c.1361C>T
AA Mutation	p.Ser454Leu(p.S454L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000494857
Start	17548743:17548743(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.598C>A
AA Mutation	p.Leu200Ile(p.L200I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000494857
Start	17551775:17551775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756005989
CDS Mutation	c.844C>T
AA Mutation	p.Arg282Trp(p.R282W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000494857
Start	17560424:17560424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1395G>T
AA Mutation	p.Gln465His(p.Q465H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000494857
Start	17561992:17561992(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1553C>T
AA Mutation	p.Ala518Val(p.A518V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000494857
Start	17543433:17543433(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376835370
CDS Mutation	c.94C>T
AA Mutation	p.Arg32Cys(p.R32C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000494857
Start	17543656:17543656(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.317C>T
AA Mutation	p.Thr106Ile(p.T106I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000494857
Start	17543652:17543652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145975234
CDS Mutation	c.313G>A
AA Mutation	p.Val105Met(p.V105M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000494857
Start	17551796:17551796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.865C>A
AA Mutation	p.Pro289Thr(p.P289T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000494857
Start	17560473:17560473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1444C>T
AA Mutation	p.Pro482Ser(p.P482S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000494857
Start	17561956:17561956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1517T>G
AA Mutation	p.Leu506Trp(p.L506W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000494857
Start	17558309:17558309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1210C>A
AA Mutation	p.Leu404Met(p.L404M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000494857
Start	17551986:17551986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1055G>A
AA Mutation	p.Ser352Asn(p.S352N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000494857
Start	17551973:17551973(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139867348
CDS Mutation	c.1042G>A
AA Mutation	p.Ala348Thr(p.A348T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000494857
Start	17562050:17562050(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767293482
CDS Mutation	c.1611C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000494857
Start	17551954:17551954(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749866127
CDS Mutation	c.1023C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000494857
Start	17565041:17565041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372948626
CDS Mutation	c.1872C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000494857
Start	17544572:17544572(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.504delT
AA Mutation	p.Phe168LeufsTer9(p.F168Lfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000494857
Start	17560494:17560494(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1465C>T
AA Mutation	p.Gln489Ter(p.Q489*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	stop_gained;inframe_insertion
Transcription ID	ENST00000494857
Start	17554661:17554662(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1157_1158insTGAATAAAA
AA Mutation	p.Thr386_Pro387insGluTerLys(p.T386_P387insE*K)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000494857
Start	17562093:17562094(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1659dupA
AA Mutation	p.Val554SerfsTer51(p.V554Sfs*51)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000494857
Start	17548817:17548818(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.672_673insATTCACCCAAG
AA Mutation	p.Leu225IlefsTer73(p.L225Ifs*73)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> SLC7A2

No Mutation Annotation!