Colon Cancer: Gene >> GAA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000302262
Start	80104839:80104839(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.253C>T
AA Mutation	p.Pro85Ser(p.P85S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000302262
Start	80117690:80117690(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2422C>T
AA Mutation	p.Pro808Ser(p.P808S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000302262
Start	80105770:80105770(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771258854
CDS Mutation	c.568C>T
AA Mutation	p.Arg190Cys(p.R190C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000302262
Start	80117600:80117600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2332G>A
AA Mutation	p.Val778Met(p.V778M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000302262
Start	80117652:80117652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2384A>G
AA Mutation	p.Glu795Gly(p.E795G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000302262
Start	80118797:80118797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756199247
CDS Mutation	c.2791G>A
AA Mutation	p.Asp931Asn(p.D931N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000302262
Start	80107592:80107592(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.728A>G
AA Mutation	p.Asp243Gly(p.D243G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000302262
Start	80117739:80117739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2471T>C
AA Mutation	p.Ile824Thr(p.I824T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000302262
Start	80110005:80110005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199748889
CDS Mutation	c.1387C>T
AA Mutation	p.Arg463Trp(p.R463W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000302262
Start	80110752:80110752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1463C>T
AA Mutation	p.Pro488Leu(p.P488L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000302262
Start	80105847:80105847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.645G>T
AA Mutation	p.Glu215Asp(p.E215D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000302262
Start	80116973:80116973(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2195C>A
AA Mutation	p.Pro732His(p.P732H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000302262
Start	80110008:80110008(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1390A>T
AA Mutation	p.Arg464Trp(p.R464W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302262
Start	80104979:80104979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.393C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000302262
Start	80104838:80104838(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.258delC
AA Mutation	p.Asn87ThrfsTer55(p.N87Tfs*55)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000302262
Start	80117015:80117015(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2242delG
AA Mutation	p.Glu748ArgfsTer16(p.E748Rfs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> GAA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000302262
Start	80108725:80108725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1223T>C
AA Mutation	p.Met408Thr(p.M408T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302262
Start	80112896:80112896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1909C>T
Mutation Classification	Silent
Feature Type	Transcript