Colon Cancer: Gene >> MEX3C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000406189
Start	51197020:51197020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.301C>T
AA Mutation	p.Pro101Ser(p.P101S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000406189
Start	51196974:51196974(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.347A>G
AA Mutation	p.Glu116Gly(p.E116G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000406189
Start	51176586:51176586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1745A>G
AA Mutation	p.Asn582Ser(p.N582S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000406189
Start	51176706:51176706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1625C>T
AA Mutation	p.Pro542Leu(p.P542L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000406189
Start	51176991:51176991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1340C>A
AA Mutation	p.Ser447Tyr(p.S447Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000406189
Start	51177503:51177503(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.828T>G
AA Mutation	p.Ile276Met(p.I276M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000406189
Start	51177519:51177519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754601042
CDS Mutation	c.812G>A
AA Mutation	p.Arg271His(p.R271H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000406189
Start	51176705:51176705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1626T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000406189
Start	51176374:51176375(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1956_1957insGTTACG
AA Mutation	p.Val651_Thr652dup(p.V651_T652dup)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> MEX3C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000406189
Start	51177431:51177431(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.900C>A
AA Mutation	p.Phe300Leu(p.F300L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript