Colon Cancer: Gene >> SLC25A14

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000218197
Start	130349337:130349337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.404G>A
AA Mutation	p.Arg135His(p.R135H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000218197
Start	130346582:130346582(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.208G>A
AA Mutation	p.Val70Ile(p.V70I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000218197
Start	130345248:130345248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.142G>A
AA Mutation	p.Gly48Ser(p.G48S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000218197
Start	130349336:130349336(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768683792
CDS Mutation	c.403C>T
AA Mutation	p.Arg135Cys(p.R135C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000218197
Start	130346581:130346581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.207G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000218197
Start	130364729:130364729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.696C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000218197
Start	130346644:130346644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772442657
CDS Mutation	c.270G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000218197
Start	130372909:130372909(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.942delT
AA Mutation	p.Phe314LeufsTer7(p.F314Lfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SLC25A14

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000218197
Start	130349295:130349295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.362A>C
AA Mutation	p.Lys121Thr(p.K121T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000218197
Start	130364661:130364661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.628G>A
AA Mutation	p.Val210Ile(p.V210I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript