ClinVar Miner

List of variants studied for chromosomal disorder by Institute for Genomic Statistics and Bioinformatics, University Hospital Bonn

Included ClinVar conditions (201):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 6
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HGVS dbSNP gnomAD frequency
NM_006940.6(SOX5):c.405dup (p.Lys136fs) rs2096571436
NM_014112.5(TRPS1):c.1630C>T (p.Arg544Ter) rs886040971
NM_014112.5(TRPS1):c.2725dup (p.Cys909fs) rs1554617582
NM_022455.5(NSD1):c.6050G>A (p.Arg2017Gln) rs587784177
NM_030665.4(RAI1):c.2966_2969del (p.Lys989fs) rs1135401792
NM_033517.1(SHANK3):c.3679dup (p.Ala1227fs) rs762292772

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