Colon Cancer: Gene >> SLC13A5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000433363
Start	6695889:6695889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.892G>A
AA Mutation	p.Ala298Thr(p.A298T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000433363
Start	6690900:6690900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1316C>T
AA Mutation	p.Pro439Leu(p.P439L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000433363
Start	6687530:6687530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1574T>C
AA Mutation	p.Met525Thr(p.M525T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000433363
Start	6690850:6690850(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146047560
CDS Mutation	c.1366G>A
AA Mutation	p.Val456Ile(p.V456I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000433363
Start	6687613:6687613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1491T>G
AA Mutation	p.Ser497Arg(p.S497R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000433363
Start	6713330:6713330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146396085
CDS Mutation	c.4G>A
AA Mutation	p.Ala2Thr(p.A2T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000433363
Start	6703048:6703048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.638G>C
AA Mutation	p.Cys213Ser(p.C213S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000433363
Start	6701097:6701097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.746A>G
AA Mutation	p.Asn249Ser(p.N249S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000433363
Start	6686316:6686316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1598A>G
AA Mutation	p.Asn533Ser(p.N533S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000433363
Start	6713261:6713261(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.73C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000433363
Start	6704035:6704035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371499002
CDS Mutation	c.390C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000433363
Start	6690881:6690881(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138802643
CDS Mutation	c.1335G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SLC13A5

No Mutation Annotation!