Details for SQSTM1:c.754+1G>T,

CHROMOSOME 5
GENOMIC COORDINATES
hg19hg38
179252227179825227
VARIANT EFFECT None
ANNOTATION FLAG None
GENE SQSTM1
REFERENCE ALLELE G
ALTERNATE ALLELE T
TRANSCRIPT NM_003900.5
CDNA CHANGE c.754+1G>T
PROTEIN CHANGE None
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
NoneNone5.356875Disease causing
DBSNP ID NA
1 combination linked to SQSTM1:c.754+1G>T, OLI1637
1 disease linked to SQSTM1:c.754+1G>T, Amyotrophic lateral sclerosis

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