Colon Cancer: Gene >> APCDD1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000355285
Start	10471700:10471700(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs537794700
CDS Mutation	c.413G>A
AA Mutation	p.Arg138Gln(p.R138Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000355285
Start	10485595:10485595(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374082304
CDS Mutation	c.908G>A
AA Mutation	p.Arg303His(p.R303H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000355285
Start	10485738:10485738(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs116815061
CDS Mutation	c.1051G>A
AA Mutation	p.Val351Ile(p.V351I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000355285
Start	10472047:10472047(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.760C>A
AA Mutation	p.Leu254Met(p.L254M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000355285
Start	10468505:10468505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.95G>T
AA Mutation	p.Ser32Ile(p.S32I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000355285
Start	10487865:10487865(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1372T>C
AA Mutation	p.Ser458Pro(p.S458P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000355285
Start	10472060:10472060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.773A>G
AA Mutation	p.Lys258Arg(p.K258R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000355285
Start	10485724:10485724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147066092
CDS Mutation	c.1037G>A
AA Mutation	p.Arg346His(p.R346H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355285
Start	10487723:10487723(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139112764
CDS Mutation	c.1230C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355285
Start	10487903:10487903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142674398
CDS Mutation	c.1410G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355285
Start	10471779:10471779(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.492C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> APCDD1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000355285
Start	10471813:10471813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs115383241
CDS Mutation	c.526G>A
AA Mutation	p.Ala176Thr(p.A176T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000355285
Start	10485583:10485583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201834801
CDS Mutation	c.896G>A
AA Mutation	p.Arg299His(p.R299H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript