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Details for IGSF10:c.352C>T, p.Arg118Ter

CHROMOSOME

3

GENOMIC COORDINATES

hg19	hg38
151171535	151453747

VARIANT EFFECT

None

ANNOTATION FLAG

None

GENE

REFERENCE ALLELE

G

ALTERNATE ALLELE

A

TRANSCRIPT

N.A.

CDNA CHANGE

c.352C>T

PROTEIN CHANGE

p.Arg118Ter

ALLELE FREQUENCY

1KGP
Global	AFR	AMR	EAS	EUR	SAS
0.0004	0.0	0.0	0.0	0.002	0.0

Gnomad
Global	AFR	AMR	ASJ	EAS	FIN	NFE	OTH	SAS
6.575e-05	0.0	0.000203	0.0	0.0	0.0	6.557e-05	0.0	8.008e-05

ESP
AA	EA
None	None

PREDICTORS

sift	pp2 hvar	cadd	mutationtaster
None	None	7.697859	Disease causing

DBSNP ID

1 combination linked to IGSF10:c.352C>T, p.Arg118Ter

1 disease linked to IGSF10:c.352C>T, p.Arg118Ter

Recurrent Pregnancy Loss

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