Details for SLC26A4:c.1150-1G>A,

CHROMOSOME 7
GENOMIC COORDINATES
hg19hg38
107330568107690123
VARIANT EFFECT splicing
ANNOTATION FLAG manually_attributed
GENE SLC26A4
REFERENCE ALLELE G
ALTERNATE ALLELE A
TRANSCRIPT NM_000441.2
CDNA CHANGE c.1150-1G>A
PROTEIN CHANGE None
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
NoneNone5.108164Disease causing
DBSNP ID NA
1 combination linked to SLC26A4:c.1150-1G>A, OLI595
1 disease linked to SLC26A4:c.1150-1G>A, Congenital hypothyroidism

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