Colon Cancer: Gene >> SPATA13

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000382095
Start	24297676:24297676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs113723819
CDS Mutation	c.1649C>T
AA Mutation	p.Ala550Val(p.A550V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000382095
Start	24286888:24286888(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.730G>A
AA Mutation	p.Val244Ile(p.V244I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000382095
Start	24302654:24302654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758752942
CDS Mutation	c.1840C>T
AA Mutation	p.Arg614Cys(p.R614C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000382095
Start	24297735:24297735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1708G>A
AA Mutation	p.Gly570Arg(p.G570R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000382095
Start	24302613:24302613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1799C>A
AA Mutation	p.Pro600His(p.P600H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000382095
Start	24294807:24294807(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1274A>G
AA Mutation	p.Lys425Arg(p.K425R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382095
Start	24284232:24284232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.387G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382095
Start	24289022:24289022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs188597102
CDS Mutation	c.816G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382095
Start	24286351:24286351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.564C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382095
Start	24284184:24284184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.339T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382095
Start	24290699:24290699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1020C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382095
Start	24294859:24294859(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1326G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382095
Start	24289172:24289172(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.966T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SPATA13

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000382095
Start	24297448:24297448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371749849
CDS Mutation	c.1421G>A
AA Mutation	p.Arg474Gln(p.R474Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript