Colon Cancer: Gene >> APLP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000221891
Start	35874768:35874768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200771936
CDS Mutation	c.1243C>T
AA Mutation	p.Arg415Cys(p.R415C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000221891
Start	35871872:35871872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.686G>C
AA Mutation	p.Arg229Pro(p.R229P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000221891
Start	35870980:35870980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.376G>A
AA Mutation	p.Gly126Ser(p.G126S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000221891
Start	35879418:35879418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1933C>T
AA Mutation	p.Arg645Cys(p.R645C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000221891
Start	35874747:35874747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775793591
CDS Mutation	c.1222C>T
AA Mutation	p.Arg408Cys(p.R408C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000221891
Start	35871349:35871349(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.537G>T
AA Mutation	p.Glu179Asp(p.E179D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000221891
Start	35871681:35871681(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375567499
CDS Mutation	c.607C>T
AA Mutation	p.Arg203Cys(p.R203C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000221891
Start	35869799:35869799(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.280T>C
AA Mutation	p.Tyr94His(p.Y94H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000221891
Start	35874853:35874853(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1328A>G
AA Mutation	p.Gln443Arg(p.Q443R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000221891
Start	35874811:35874811(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs568306221
CDS Mutation	c.1286G>A
AA Mutation	p.Arg429His(p.R429H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000221891
Start	35878903:35878903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1664T>C
AA Mutation	p.Val555Ala(p.V555A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000221891
Start	35874845:35874845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1320G>T
AA Mutation	p.Glu440Asp(p.E440D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000221891
Start	35871269:35871269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.457C>T
AA Mutation	p.Pro153Ser(p.P153S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000221891
Start	35871968:35871968(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777735772
CDS Mutation	c.782C>T
AA Mutation	p.Pro261Leu(p.P261L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000221891
Start	35879137:35879137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1777G>A
AA Mutation	p.Gly593Arg(p.G593R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000221891
Start	35873645:35873645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.988C>T
AA Mutation	p.Arg330Cys(p.R330C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000221891
Start	35878931:35878931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762155649
CDS Mutation	c.1692G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000221891
Start	35871882:35871882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.696C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000221891
Start	35871680:35871680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.606C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	stop_gained
Transcription ID	ENST00000221891
Start	35874552:35874552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1105C>T
AA Mutation	p.Arg369Ter(p.R369*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000221891
Start	35879073:35879073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1714-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> APLP1

No Mutation Annotation!