Colon Cancer: Gene >> SPATA18

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000295213
Start	52084958:52084958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1522T>G
AA Mutation	p.Leu508Val(p.L508V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000295213
Start	52072099:52072099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139201868
CDS Mutation	c.701G>A
AA Mutation	p.Arg234Gln(p.R234Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000295213
Start	52094546:52094546(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1583C>A
AA Mutation	p.Pro528His(p.P528H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000295213
Start	52071949:52071949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142158631
CDS Mutation	c.551G>A
AA Mutation	p.Arg184His(p.R184H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000295213
Start	52076930:52076930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.910T>C
AA Mutation	p.Ser304Pro(p.S304P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295213
Start	52082408:52082408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs137981042
CDS Mutation	c.1377G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295213
Start	52084975:52084975(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773192989
CDS Mutation	c.1539C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295213
Start	52060825:52060825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.237G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SPATA18

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000295213
Start	52078889:52078889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1175T>C
AA Mutation	p.Val392Ala(p.V392A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000295213
Start	52072110:52072110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.712G>A
AA Mutation	p.Glu238Lys(p.E238K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295213
Start	52051710:52051710(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6G>C
Mutation Classification	Silent
Feature Type	Transcript