ClinVar Miner

List of variants in gene NBN reported as uncertain significance by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 14
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HGVS dbSNP
NM_002485.4(NBN):c.-26G>A rs201392451
NM_002485.4(NBN):c.1023C>G (p.Ser341Arg) rs756023239
NM_002485.4(NBN):c.1125-3C>T rs587781326
NM_002485.4(NBN):c.1205_1209del (p.Thr402fs) rs1563532144
NM_002485.4(NBN):c.1262T>C (p.Leu421Ser) rs104895032
NM_002485.4(NBN):c.1383G>A (p.Pro461=) rs886063169
NM_002485.4(NBN):c.1444A>G (p.Arg482Gly) rs886063168
NM_002485.4(NBN):c.172-3C>T rs587781620
NM_002485.4(NBN):c.1909_1910delinsTA (p.Ile637Ter) rs1563516254
NM_002485.4(NBN):c.1925A>G (p.Lys642Arg) rs587781547
NM_002485.4(NBN):c.2146A>G (p.Asn716Asp) rs72563785
NM_002485.4(NBN):c.37+10G>C rs369408590
NM_002485.4(NBN):c.505C>T (p.Arg169Cys) rs182756889
NM_002485.4(NBN):c.596C>G (p.Pro199Arg) rs730881844

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