Colon Cancer: Gene >> DNA2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358410
Start	68432255:68432255(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1824T>G
AA Mutation	p.Ser608Arg(p.S608R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000358410
Start	68459156:68459156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.667G>T
AA Mutation	p.Asp223Tyr(p.D223Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000358410
Start	68422778:68422778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2321G>C
AA Mutation	p.Gly774Ala(p.G774A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000358410
Start	68468287:68468287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.277C>T
AA Mutation	p.Pro93Ser(p.P93S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000358410
Start	68419125:68419125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2876G>T
AA Mutation	p.Gly959Val(p.G959V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000358410
Start	68468236:68468236(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.328A>T
AA Mutation	p.Ile110Leu(p.I110L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000358410
Start	68445057:68445057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1084G>A
AA Mutation	p.Ala362Thr(p.A362T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000358410
Start	68415064:68415064(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3158T>C
AA Mutation	p.Ile1053Thr(p.I1053T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000358410
Start	68416715:68416715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3108A>C
AA Mutation	p.Glu1036Asp(p.E1036D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000358410
Start	68419117:68419117(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2884G>A
AA Mutation	p.Glu962Lys(p.E962K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358410
Start	68432402:68432402(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs577208486
CDS Mutation	c.1755G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358410
Start	68419884:68419884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371684850
CDS Mutation	c.2706G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358410
Start	68442922:68442922(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145280717
CDS Mutation	c.1410G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358410
Start	68430553:68430554(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2090dupT
AA Mutation	p.Leu697PhefsTer28(p.L697Ffs*28)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> DNA2

No Mutation Annotation!