Colon Cancer: Gene >> MFAP3L

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361618
Start	169991427:169991427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1181C>T
AA Mutation	p.Ala394Val(p.A394V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361618
Start	169991989:169991989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.619C>T
AA Mutation	p.Arg207Cys(p.R207C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361618
Start	169992186:169992186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.422G>A
AA Mutation	p.Arg141His(p.R141H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000361618
Start	169991724:169991724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759421553
CDS Mutation	c.884G>A
AA Mutation	p.Arg295Gln(p.R295Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000361618
Start	169991991:169991991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.617A>T
AA Mutation	p.Lys206Met(p.K206M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000361618
Start	169991995:169991995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759625030
CDS Mutation	c.613G>A
AA Mutation	p.Ala205Thr(p.A205T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361618
Start	169992110:169992110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.498C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361618
Start	169991483:169991483(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1125T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361618
Start	170005725:170005725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.153C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361618
Start	169991696:169991696(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377059924
CDS Mutation	c.912C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000361618
Start	169991806:169991806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.802C>T
AA Mutation	p.Gln268Ter(p.Q268*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> MFAP3L

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361618
Start	169992041:169992041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.567C>A
AA Mutation	p.Phe189Leu(p.F189L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361618
Start	169991719:169991719(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.889G>T
AA Mutation	p.Asp297Tyr(p.D297Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361618
Start	169991381:169991381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1227C>A
Mutation Classification	Silent
Feature Type	Transcript