Colon Cancer: Gene >> SUSD2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358321
Start	24187738:24187738(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2059C>A
AA Mutation	p.His687Asn(p.H687N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000358321
Start	24188282:24188282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377355379
CDS Mutation	c.2399C>T
AA Mutation	p.Ala800Val(p.A800V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000358321
Start	24184264:24184264(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.568C>A
AA Mutation	p.Gln190Lys(p.Q190K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000358321
Start	24186114:24186114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143852867
CDS Mutation	c.1438G>A
AA Mutation	p.Asp480Asn(p.D480N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000358321
Start	24183613:24183613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.406C>G
AA Mutation	p.His136Asp(p.H136D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000358321
Start	24187727:24187727(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2048G>A
AA Mutation	p.Cys683Tyr(p.C683Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000358321
Start	24187345:24187345(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1786C>A
AA Mutation	p.Leu596Ile(p.L596I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000358321
Start	24186130:24186130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs116820424
CDS Mutation	c.1454C>T
AA Mutation	p.Ala485Val(p.A485V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000358321
Start	24184279:24184279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.583G>A
AA Mutation	p.Glu195Lys(p.E195K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358321
Start	24183088:24183088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149912020
CDS Mutation	c.108C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358321
Start	24184179:24184179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.483G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358321
Start	24185247:24185247(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.936C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358321
Start	24187605:24187605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150529613
CDS Mutation	c.1926C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358321
Start	24184209:24184209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.513C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358321
Start	24185917:24185917(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1331delC
AA Mutation	p.Pro444GlnfsTer13(p.P444Qfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SUSD2

No Mutation Annotation!