Colon Cancer: Gene >> FAM161B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000286544
Start	73944808:73944808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776741915
CDS Mutation	c.641C>T
AA Mutation	p.Ser214Leu(p.S214L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000286544
Start	73938014:73938014(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754779063
CDS Mutation	c.1688G>A
AA Mutation	p.Arg563His(p.R563H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000286544
Start	73946317:73946317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.532A>G
AA Mutation	p.Met178Val(p.M178V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000286544
Start	73946325:73946325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.524A>G
AA Mutation	p.Asp175Gly(p.D175G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000286544
Start	73946332:73946332(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.517G>T
AA Mutation	p.Asp173Tyr(p.D173Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000286544
Start	73942532:73942532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1298C>T
AA Mutation	p.Pro433Leu(p.P433L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000286544
Start	73942415:73942415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779578513
CDS Mutation	c.1415G>A
AA Mutation	p.Arg472His(p.R472H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000286544
Start	73937628:73937628(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1828C>T
AA Mutation	p.Pro610Ser(p.P610S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000286544
Start	73944549:73944549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142518976
CDS Mutation	c.900C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000286544
Start	73946478:73946479(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.370dupT
AA Mutation	p.Ser124PhefsTer2(p.S124Ffs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000286544
Start	73938094:73938095(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1607dupA
AA Mutation	p.Asn537GlufsTer5(p.N537Efs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> FAM161B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000286544
Start	73937642:73937642(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs571286955
CDS Mutation	c.1814G>A
AA Mutation	p.Arg605Gln(p.R605Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000286544
Start	73941001:73941001(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1514G>A
AA Mutation	p.Gly505Asp(p.G505D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000286544
Start	73941014:73941014(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1501C>G
AA Mutation	p.Arg501Gly(p.R501G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000286544
Start	73942695:73942695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1135A>C
AA Mutation	p.Ile379Leu(p.I379L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript