Details for DUOX2:c.2148+1G>T,

CHROMOSOME 15
GENOMIC COORDINATES
hg19hg38
4539832245106124
VARIANT EFFECT splicing
ANNOTATION FLAG manually_attributed
GENE DUOX2
REFERENCE ALLELE C
ALTERNATE ALLELE A
TRANSCRIPT NM_014080
CDNA CHANGE c.2148+1G>T
PROTEIN CHANGE None
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
NoneNone5.718091Disease causing
DBSNP ID rs1566975448
1 combination linked to DUOX2:c.2148+1G>T, OLI567
1 disease linked to DUOX2:c.2148+1G>T, Congenital hypothyroidism

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