Colon Cancer: Gene >> MUC20

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000447234
Start	195725771:195725771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs565436915
CDS Mutation	c.1168G>A
AA Mutation	p.Asp390Asn(p.D390N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000447234
Start	195724998:195724998(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.395G>T
AA Mutation	p.Gly132Val(p.G132V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000447234
Start	195725174:195725174(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.571C>T
AA Mutation	p.Arg191Trp(p.R191W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000447234
Start	195721035:195721035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773516940
CDS Mutation	c.28C>T
AA Mutation	p.Pro10Ser(p.P10S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000447234
Start	195726255:195726255(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368331468
CDS Mutation	c.1652C>T
AA Mutation	p.Pro551Leu(p.P551L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000447234
Start	195724946:195724946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs528684754
CDS Mutation	c.343G>A
AA Mutation	p.Ala115Thr(p.A115T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000447234
Start	195726105:195726105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1502C>A
AA Mutation	p.Pro501His(p.P501H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000447234
Start	195725961:195725961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1358C>T
AA Mutation	p.Ser453Leu(p.S453L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000447234
Start	195726499:195726499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374691440
CDS Mutation	c.1896G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000447234
Start	195726115:195726115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769720088
CDS Mutation	c.1512C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000447234
Start	195726262:195726262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1659C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> MUC20

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000447234
Start	195725908:195725908(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1305C>T
Mutation Classification	Silent
Feature Type	Transcript