Colon Cancer: Gene >> SLC25A13

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265631
Start	96131755:96131755(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1579G>A
AA Mutation	p.Gly527Ser(p.G527S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265631
Start	96146654:96146654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143877538
CDS Mutation	c.1354G>A
AA Mutation	p.Val452Ile(p.V452I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265631
Start	96184337:96184337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1117A>G
AA Mutation	p.Asn373Asp(p.N373D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265631
Start	96277284:96277284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.124A>T
AA Mutation	p.Thr42Ser(p.T42S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265631
Start	96131841:96131841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1493C>T
AA Mutation	p.Ala498Val(p.A498V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000265631
Start	96121878:96121878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753626243
CDS Mutation	c.1711C>T
AA Mutation	p.Arg571Cys(p.R571C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000265631
Start	96189376:96189376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771117913
CDS Mutation	c.851G>A
AA Mutation	p.Arg284His(p.R284H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000265631
Start	96184411:96184411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1043C>A
AA Mutation	p.Pro348His(p.P348H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000265631
Start	96184947:96184947(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.998G>A
AA Mutation	p.Gly333Asp(p.G333D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265631
Start	96193166:96193166(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.486C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265631
Start	96131861:96131861(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1473G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265631
Start	96208859:96208859(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760730497
CDS Mutation	c.447G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000265631
Start	96184352:96184352(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1102G>T
AA Mutation	p.Glu368Ter(p.E368*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SLC25A13

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265631
Start	96191163:96191163(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.700A>G
AA Mutation	p.Arg234Gly(p.R234G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265631
Start	96208901:96208901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768953296
CDS Mutation	c.405A>C
AA Mutation	p.Gln135His(p.Q135H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265631
Start	96170082:96170082(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1274C>T
AA Mutation	p.Ser425Leu(p.S425L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265631
Start	96191212:96191212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.651C>A
AA Mutation	p.Phe217Leu(p.F217L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript