Details for COL4A4:c.5026C>T, p.Gln1676Ter

CHROMOSOME 2
GENOMIC COORDINATES
hg19hg38
227872088227007372
VARIANT EFFECT nonsense
ANNOTATION FLAG automatically_attributed
GENE COL4A4
REFERENCE ALLELE G
ALTERNATE ALLELE A
TRANSCRIPT NM_000092.4
CDNA CHANGE c.5026C>T
PROTEIN CHANGE p.Gln1676Ter
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
NoneNone8.066921Disease causing
DBSNP ID NA
1 combination linked to COL4A4:c.5026C>T, p.Gln1676Ter OLI034
1 disease linked to COL4A4:c.5026C>T, p.Gln1676Ter Alport syndrome

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