Colon Cancer: Gene >> MUC21

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376296
Start	30987329:30987329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1154G>A
AA Mutation	p.Ser385Asn(p.S385N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000376296
Start	30986893:30986893(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.718G>A
AA Mutation	p.Ala240Thr(p.A240T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000376296
Start	30988055:30988055(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767452922
CDS Mutation	c.1562G>A
AA Mutation	p.Gly521Asp(p.G521D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000376296
Start	30986497:30986497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.322T>C
AA Mutation	p.Ser108Pro(p.S108P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000376296
Start	30986668:30986668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.493G>A
AA Mutation	p.Ala165Thr(p.A165T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000376296
Start	30986737:30986737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780528569
CDS Mutation	c.562G>A
AA Mutation	p.Val188Met(p.V188M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000376296
Start	30987644:30987644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761798063
CDS Mutation	c.1469C>T
AA Mutation	p.Ala490Val(p.A490V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000376296
Start	30983986:30983986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146848216
CDS Mutation	c.28C>A
AA Mutation	p.Leu10Ile(p.L10I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000376296
Start	30986933:30986933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.758G>A
AA Mutation	p.Gly253Asp(p.G253D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376296
Start	30986466:30986466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373319157
CDS Mutation	c.291A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376296
Start	30986892:30986892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.717A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376296
Start	30986796:30986796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.621C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376296
Start	30987528:30987528(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1353T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> MUC21

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376296
Start	30987645:30987645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368460700
CDS Mutation	c.1470G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376296
Start	30986826:30986826(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs532108366
CDS Mutation	c.651G>A
Mutation Classification	Silent
Feature Type	Transcript