Details for TULP3:c.709G>T, p.Ala237Ser

CHROMOSOME 12
GENOMIC COORDINATES
hg19hg38
30425962933430
VARIANT EFFECT missense
ANNOTATION FLAG automatically_attributed
GENE TULP3
REFERENCE ALLELE G
ALTERNATE ALLELE T
TRANSCRIPT NM_003324.4
CDNA CHANGE c.709G>T
PROTEIN CHANGE p.Ala237Ser
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
3.981e-060.00.00.00.00.00.00.03.269e-05

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
DeleteriousDamaging4.092565Polymorphism
DBSNP ID rs762869650
1 combination linked to TULP3:c.709G>T, p.Ala237Ser OLI714
1 disease linked to TULP3:c.709G>T, p.Ala237Ser Isolated anencephaly

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