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Details for DHX37:c.1399C>G, p.Leu467Val

CHROMOSOME

12

GENOMIC COORDINATES

hg19	hg38
125453089	124968543

VARIANT EFFECT

None

ANNOTATION FLAG

None

GENE

REFERENCE ALLELE

G

ALTERNATE ALLELE

C

TRANSCRIPT

CDNA CHANGE

c.1399C>G

PROTEIN CHANGE

p.Leu467Val

ALLELE FREQUENCY

1KGP
Global	AFR	AMR	EAS	EUR	SAS
0.0002	0.0008	0.0	0.0	0.0	0.0

Gnomad
Global	AFR	AMR	ASJ	EAS	FIN	NFE	OTH	SAS
0.000188	0.0	0.0002314	0.0	0.0	0.0	0.0002913	0.0001635	0.0001633

ESP
AA	EA
None	None

PREDICTORS

sift	pp2 hvar	cadd	mutationtaster
Deleterious	Damaging	2.655901	Disease causing

DBSNP ID

1 combination linked to DHX37:c.1399C>G, p.Leu467Val

1 disease linked to DHX37:c.1399C>G, p.Leu467Val

46,XY disorder of sex development

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