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Details for FLRT1:c.1184C>T, p.Thr395Met

CHROMOSOME

11

GENOMIC COORDINATES

hg19	hg38
63884923	64117451

VARIANT EFFECT

missense

ANNOTATION FLAG

automatically_attributed

GENE

REFERENCE ALLELE

C

ALTERNATE ALLELE

T

TRANSCRIPT

CDNA CHANGE

c.1184C>T

PROTEIN CHANGE

p.Thr395Met

ALLELE FREQUENCY

1KGP
Global	AFR	AMR	EAS	EUR	SAS
0.0016	0.0	0.0014	0.0	0.005	0.002

Gnomad
Global	AFR	AMR	ASJ	EAS	FIN	NFE	OTH	SAS
0.001514	0.0001868	0.0004637	0.0	0.0	0.001267	0.002297	0.001647	0.002062

ESP
AA	EA
0.0004543	0.00291

PREDICTORS

sift	pp2 hvar	cadd	mutationtaster
Tolerated	Damaging	2.575564	Polymorphism

DBSNP ID

1 combination linked to FLRT1:c.1184C>T, p.Thr395Met

1 disease linked to FLRT1:c.1184C>T, p.Thr395Met

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