Colon Cancer: Gene >> TOPORS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000360538
Start	32542997:32542997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1528A>G
AA Mutation	p.Met510Val(p.M510V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000360538
Start	32543746:32543746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.779G>A
AA Mutation	p.Arg260Gln(p.R260Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000360538
Start	32544016:32544016(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.509C>A
AA Mutation	p.Ser170Tyr(p.S170Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000360538
Start	32542036:32542036(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2489C>T
AA Mutation	p.Ser830Leu(p.S830L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000360538
Start	32543903:32543903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.622G>A
AA Mutation	p.Asp208Asn(p.D208N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000360538
Start	32542465:32542465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2060G>T
AA Mutation	p.Arg687Ile(p.R687I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000360538
Start	32542037:32542037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2488T>C
AA Mutation	p.Ser830Pro(p.S830P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000360538
Start	32543410:32543410(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1115C>T
AA Mutation	p.Ala372Val(p.A372V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360538
Start	32542377:32542377(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs534139603
CDS Mutation	c.2148C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360538
Start	32543331:32543331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747437233
CDS Mutation	c.1194G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360538
Start	32542179:32542179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777159758
CDS Mutation	c.2346C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360538
Start	32543904:32543904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748364310
CDS Mutation	c.621G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000360538
Start	32544124:32544124(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.401delA
AA Mutation	p.Asn134ThrfsTer19(p.N134Tfs*19)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000360538
Start	32542139:32542139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2386C>T
AA Mutation	p.Arg796Ter(p.R796*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000360538
Start	32543486:32543486(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1039C>T
AA Mutation	p.Arg347Ter(p.R347*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TOPORS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000360538
Start	32543129:32543129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755081657
CDS Mutation	c.1396G>A
AA Mutation	p.Asp466Asn(p.D466N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000360538
Start	32543429:32543429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1096G>T
AA Mutation	p.Ala366Ser(p.A366S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000360538
Start	32542672:32542672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1853A>G
AA Mutation	p.His618Arg(p.H618R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000360538
Start	32542528:32542528(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1997G>A
AA Mutation	p.Ser666Asn(p.S666N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000360538
Start	32542596:32542596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1929A>C
AA Mutation	p.Lys643Asn(p.K643N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000360538
Start	32543406:32543406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1119T>G
AA Mutation	p.Asn373Lys(p.N373K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript