Colon Cancer: Gene >> MUC15

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000455601
Start	26565678:26565678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.181A>C
AA Mutation	p.Asn61His(p.N61H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000455601
Start	26565443:26565443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs72877805
CDS Mutation	c.416A>G
AA Mutation	p.Asn139Ser(p.N139S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000455601
Start	26565369:26565369(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.490A>G
AA Mutation	p.Ser164Gly(p.S164G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000455601
Start	26565577:26565577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.282G>C
AA Mutation	p.Glu94Asp(p.E94D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000455601
Start	26565555:26565555(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs563199813
CDS Mutation	c.304C>A
AA Mutation	p.Pro102Thr(p.P102T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000455601
Start	26563142:26563142(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745838488
CDS Mutation	c.818G>A
AA Mutation	p.Arg273Gln(p.R273Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000455601
Start	26565168:26565168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.691A>C
AA Mutation	p.Lys231Gln(p.K231Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000455601
Start	26563162:26563162(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764780529
CDS Mutation	c.798G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000455601
Start	26565802:26565802(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370334569
CDS Mutation	c.57G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000455601
Start	26565667:26565667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.192C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000455601
Start	26563240:26563240(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761084763
CDS Mutation	c.720C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> MUC15

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000455601
Start	26563142:26563142(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745838488
CDS Mutation	c.818G>A
AA Mutation	p.Arg273Gln(p.R273Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000455601
Start	26565777:26565777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.82G>T
AA Mutation	p.Asp28Tyr(p.D28Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000455601
Start	26565538:26565538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.321C>A
Mutation Classification	Silent
Feature Type	Transcript