Colon Cancer: Gene >> FARSB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000281828
Start	222633226:222633226(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139596776
CDS Mutation	c.688G>A
AA Mutation	p.Val230Ile(p.V230I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000281828
Start	222571991:222571991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1650G>T
AA Mutation	p.Glu550Asp(p.E550D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000281828
Start	222648743:222648743(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.111A>C
AA Mutation	p.Glu37Asp(p.E37D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000281828
Start	222642951:222642951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.169G>A
AA Mutation	p.Ala57Thr(p.A57T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000281828
Start	222630149:222630149(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.812T>C
AA Mutation	p.Val271Ala(p.V271A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000281828
Start	222634445:222634445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.552G>T
AA Mutation	p.Lys184Asn(p.K184N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000281828
Start	222571953:222571953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1688T>C
AA Mutation	p.Val563Ala(p.V563A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000281828
Start	222613823:222613823(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1450G>T
AA Mutation	p.Asp484Tyr(p.D484Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000281828
Start	222656030:222656030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.44T>C
AA Mutation	p.Leu15Pro(p.L15P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000281828
Start	222599961:222599961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1585G>T
AA Mutation	p.Asp529Tyr(p.D529Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000281828
Start	222648791:222648791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141065703
CDS Mutation	c.63C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000281828
Start	222630168:222630168(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.793delA
AA Mutation	p.Ile265Ter(p.I265*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000281828
Start	222600064:222600064(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1482C>G
AA Mutation	p.Tyr494Ter(p.Y494*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000281828
Start	222624353:222624354(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1088_1089insCAATAAGGAGTGTT
AA Mutation	p.Ile364AsnfsTer7(p.I364Nfs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000281828
Start	222600003:222600004(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1542_1543insTCACTAACT
AA Mutation	p.Leu514_Leu515insSerLeuThr(p.L514_L515insSLT)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> FARSB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000281828
Start	222642997:222642997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.123G>T
AA Mutation	p.Glu41Asp(p.E41D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000281828
Start	222624478:222624478(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.964G>T
AA Mutation	p.Glu322Ter(p.E322*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript