Colon Cancer: Gene >> RASA3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000334062
Start	114015296:114015296(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370539205
CDS Mutation	c.1318G>A
AA Mutation	p.Ala440Thr(p.A440T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000334062
Start	114011238:114011238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200485426
CDS Mutation	c.1523C>T
AA Mutation	p.Thr508Met(p.T508M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000334062
Start	113996705:113996705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1967A>G
AA Mutation	p.Tyr656Cys(p.Y656C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000334062
Start	114029823:114029823(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.437A>C
AA Mutation	p.Lys146Thr(p.K146T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000334062
Start	114018176:114018176(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757728151
CDS Mutation	c.1019G>A
AA Mutation	p.Arg340Gln(p.R340Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000334062
Start	114021492:114021492(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779182286
CDS Mutation	c.697G>A
AA Mutation	p.Ala233Thr(p.A233T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000334062
Start	114018858:114018858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.847C>A
AA Mutation	p.Leu283Met(p.L283M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000334062
Start	113992535:113992535(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs188598762
CDS Mutation	c.2195G>A
AA Mutation	p.Arg732His(p.R732H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000334062
Start	113999604:113999604(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753088536
CDS Mutation	c.1913A>C
AA Mutation	p.Glu638Ala(p.E638A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000334062
Start	114018881:114018881(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.824T>C
AA Mutation	p.Leu275Pro(p.L275P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000334062
Start	114013176:114013176(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1478C>T
AA Mutation	p.Ser493Phe(p.S493F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000334062
Start	113996715:113996715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1957C>T
AA Mutation	p.Arg653Cys(p.R653C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334062
Start	114027864:114027864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs575958394
CDS Mutation	c.513G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334062
Start	114011237:114011237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202142638
CDS Mutation	c.1524G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000334062
Start	114021426:114021426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.763C>T
AA Mutation	p.Gln255Ter(p.Q255*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> RASA3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000334062
Start	114009397:114009397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755498753
CDS Mutation	c.1658C>T
AA Mutation	p.Ala553Val(p.A553V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000334062
Start	114009434:114009434(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1621T>G
AA Mutation	p.Phe541Val(p.F541V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000334062
Start	114024286:114024286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370747207
CDS Mutation	c.673G>A
AA Mutation	p.Glu225Lys(p.E225K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000334062
Start	114073811:114073811(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.82C>T
AA Mutation	p.Pro28Ser(p.P28S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334062
Start	114018199:114018199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.996G>A
Mutation Classification	Silent
Feature Type	Transcript