Colon Cancer: Gene >> SLC9A2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000233969
Start	102665341:102665341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.995G>A
AA Mutation	p.Gly332Asp(p.G332D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000233969
Start	102657755:102657755(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.481C>A
AA Mutation	p.Pro161Thr(p.P161T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000233969
Start	102658013:102658013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.739G>T
AA Mutation	p.Asp247Tyr(p.D247Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000233969
Start	102702477:102702477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1820G>T
AA Mutation	p.Arg607Ile(p.R607I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000233969
Start	102708362:102708362(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2312A>G
AA Mutation	p.Asp771Gly(p.D771G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000233969
Start	102708128:102708128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2078G>A
AA Mutation	p.Ser693Asn(p.S693N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000233969
Start	102657896:102657896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.622C>G
AA Mutation	p.Leu208Val(p.L208V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000233969
Start	102702439:102702439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374054836
CDS Mutation	c.1782G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000233969
Start	102657757:102657757(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.483A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000233969
Start	102619970:102619970(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.124delG
AA Mutation	p.Ala42ProfsTer66(p.A42Pfs*66)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	protein_altering_variant
Transcription ID	ENST00000233969
Start	102657894:102657895(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.620_621insAAT
AA Mutation	p.Asn207delinsLysIle(p.N207delinsKI)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> SLC9A2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000233969
Start	102683367:102683367(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1111G>A
AA Mutation	p.Glu371Lys(p.E371K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000233969
Start	102657892:102657892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.618G>T
AA Mutation	p.Gln206His(p.Q206H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript