Colon Cancer: Gene >> FAM120A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000277165
Start	93550584:93550584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2167G>T
AA Mutation	p.Val723Leu(p.V723L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000277165
Start	93452274:93452274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.359A>T
AA Mutation	p.Gln120Leu(p.Q120L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000277165
Start	93516211:93516211(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1360C>A
AA Mutation	p.Pro454Thr(p.P454T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000277165
Start	93529420:93529420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1574C>A
AA Mutation	p.Thr525Asn(p.T525N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000277165
Start	93557918:93557918(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746136202
CDS Mutation	c.2576C>T
AA Mutation	p.Pro859Leu(p.P859L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000277165
Start	93516074:93516074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1223G>A
AA Mutation	p.Ser408Asn(p.S408N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000277165
Start	93564312:93564312(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3129G>C
AA Mutation	p.Met1043Ile(p.M1043I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000277165
Start	93527169:93527169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1433A>G
AA Mutation	p.Asn478Ser(p.N478S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000277165
Start	93556539:93556539(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2432T>C
AA Mutation	p.Leu811Pro(p.L811P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000277165
Start	93452329:93452329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.414C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000277165
Start	93529496:93529496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150866667
CDS Mutation	c.1650C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000277165
Start	93556426:93556426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2319C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000277165
Start	93471218:93471218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758630108
CDS Mutation	c.552G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000277165
Start	93529532:93529532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1686G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000277165
Start	93550649:93550649(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2232G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000277165
Start	93529491:93529491(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1650delC
AA Mutation	p.Val551SerfsTer6(p.V551Sfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000277165
Start	93562218:93562218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2959G>T
AA Mutation	p.Gly987Ter(p.G987*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000277165
Start	93527216:93527216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1480C>T
AA Mutation	p.Arg494Ter(p.R494*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> FAM120A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000277165
Start	93497474:93497474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.808C>T
AA Mutation	p.Arg270Trp(p.R270W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000277165
Start	93556469:93556469(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2362G>A
AA Mutation	p.Gly788Arg(p.G788R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000277165
Start	93498824:93498824(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.968G>T
AA Mutation	p.Arg323Ile(p.R323I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000277165
Start	93516121:93516121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1270G>A
AA Mutation	p.Glu424Lys(p.E424K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000277165
Start	93561126:93561126(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2824T>C
AA Mutation	p.Ser942Pro(p.S942P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000277165
Start	93529577:93529577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769862112
CDS Mutation	c.1731G>A
Mutation Classification	Silent
Feature Type	Transcript