Colon Cancer: Gene >> MUC13

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000616727
Start	124912116:124912116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777698206
CDS Mutation	c.1240G>A
AA Mutation	p.Asp414Asn(p.D414N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000616727
Start	124916337:124916337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.944G>A
AA Mutation	p.Ser315Asn(p.S315N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000616727
Start	124910464:124910464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142060793
CDS Mutation	c.1288G>A
AA Mutation	p.Ala430Thr(p.A430T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000616727
Start	124916452:124916452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368207084
CDS Mutation	c.829C>T
AA Mutation	p.Arg277Cys(p.R277C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000616727
Start	124913673:124913673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758163036
CDS Mutation	c.973C>T
AA Mutation	p.Arg325Trp(p.R325W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000616727
Start	124908286:124908286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1400T>G
AA Mutation	p.Leu467Arg(p.L467R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000616727
Start	124916381:124916381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.900G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000616727
Start	124908234:124908234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1452T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000616727
Start	124908333:124908333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs562055720
CDS Mutation	c.1353G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000616727
Start	124927782:124927782(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.264C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000616727
Start	124913122:124913122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745450880
CDS Mutation	c.1203G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000616727
Start	124927578:124927578(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.468T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000616727
Start	124927782:124927782(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.264delC
AA Mutation	p.Ile89Ter(p.I89*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> MUC13

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000616727
Start	124927933:124927933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.113C>A
AA Mutation	p.Pro38His(p.P38H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000616727
Start	124912120:124912120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1236A>C
Mutation Classification	Silent
Feature Type	Transcript