Colon Cancer: Gene >> FAM107B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000378458
Start	14521243:14521243(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.343A>G
AA Mutation	p.Lys115Glu(p.K115E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000181796
Start	14774317:14774317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763943353
CDS Mutation	c.347C>T
AA Mutation	p.Ala116Val(p.A116V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000181796
Start	14774495:14774495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.169G>A
AA Mutation	p.Val57Met(p.V57M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000181796
Start	14774461:14774461(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767708669
CDS Mutation	c.203G>A
AA Mutation	p.Ser68Asn(p.S68N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000181796
Start	14774260:14774260(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs151236833
CDS Mutation	c.404C>T
AA Mutation	p.Thr135Met(p.T135M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000378458
Start	14521889:14521889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757704900
CDS Mutation	c.259C>T
AA Mutation	p.Arg87Trp(p.R87W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> FAM107B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000378458
Start	14521227:14521227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.359G>A
AA Mutation	p.Arg120Lys(p.R120K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000181796
Start	14774378:14774378(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs545803258
CDS Mutation	c.286C>T
AA Mutation	p.Arg96Cys(p.R96C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000181796
Start	14667658:14667658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766482832
CDS Mutation	c.445G>A
AA Mutation	p.Glu149Lys(p.E149K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000378458
Start	14521227:14521227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.359G>T
AA Mutation	p.Arg120Ile(p.R120I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378458
Start	14522001:14522001(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.147C>T
Mutation Classification	Silent
Feature Type	Transcript