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Details for MCM2:c.1670C>G, p.Thr557Arg

CHROMOSOME

3

GENOMIC COORDINATES

hg19	hg38
127335858	127617015

VARIANT EFFECT

None

ANNOTATION FLAG

None

GENE

REFERENCE ALLELE

C

ALTERNATE ALLELE

G

TRANSCRIPT

N.A.

CDNA CHANGE

c.1670C>G

PROTEIN CHANGE

p.Thr557Arg

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
None	None	None	None	None	None	None	None	None

ESP
AA	EA
None	None

PREDICTORS

sift	pp2 hvar	cadd	mutationtaster
Deleterious	Damaging	3.893891	Disease causing

DBSNP ID

1 combination linked to MCM2:c.1670C>G, p.Thr557Arg

1 disease linked to MCM2:c.1670C>G, p.Thr557Arg

Recurrent Pregnancy Loss

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