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Details for KLHL7:c.1258C>T, p.Arg420Cys

CHROMOSOME

7

GENOMIC COORDINATES

hg19	hg38
23207535	23167916

VARIANT EFFECT

missense

ANNOTATION FLAG

automatically_attributed

GENE

REFERENCE ALLELE

C

ALTERNATE ALLELE

T

TRANSCRIPT

CDNA CHANGE

c.1258C>T

PROTEIN CHANGE

p.Arg420Cys

ALLELE FREQUENCY

1KGP
Global	AFR	AMR	EAS	EUR	SAS
None	None	None	None	None	None

Gnomad
Global	AFR	AMR	ASJ	EAS	FIN	NFE	OTH	SAS
7.953e-06	0.0	0.0	0.0	5.437e-05	0.0	8.791e-06	0.0	0.0

ESP
AA	EA
None	None

PREDICTORS

sift	pp2 hvar	cadd	mutationtaster
Deleterious	Damaging	4.471855	Disease causing

DBSNP ID

1 combination linked to KLHL7:c.1258C>T, p.Arg420Cys

1 disease linked to KLHL7:c.1258C>T, p.Arg420Cys

Arthrogryposis syndrome

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