ClinVar Miner

List of variants in gene PCNT reported as likely benign by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 33
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HGVS dbSNP
NM_006031.6(PCNT):c.*101T>G rs138450666
NM_006031.6(PCNT):c.*343_*346del rs145379994
NM_006031.6(PCNT):c.-25G>C rs202239640
NM_006031.6(PCNT):c.1040A>G (p.Lys347Arg) rs80166001
NM_006031.6(PCNT):c.1519C>G (p.Arg507Gly) rs138036524
NM_006031.6(PCNT):c.1784C>T (p.Ala595Val) rs143028464
NM_006031.6(PCNT):c.2033A>G (p.Lys678Arg) rs149623054
NM_006031.6(PCNT):c.2264T>G (p.Met755Arg) rs201827977
NM_006031.6(PCNT):c.2865C>T (p.Ala955=) rs540548340
NM_006031.6(PCNT):c.3698A>C (p.Glu1233Ala)
NM_006031.6(PCNT):c.3748C>T (p.Arg1250Trp) rs117987006
NM_006031.6(PCNT):c.4142C>T (p.Ala1381Val) rs114383833
NM_006031.6(PCNT):c.4285C>T (p.Arg1429Cys) rs62224222
NM_006031.6(PCNT):c.4345C>G (p.Gln1449Glu) rs139432601
NM_006031.6(PCNT):c.4571C>G (p.Pro1524Arg) rs35513449
NM_006031.6(PCNT):c.5724G>A (p.Gln1908=)
NM_006031.6(PCNT):c.5826G>A (p.Arg1942=) rs536281306
NM_006031.6(PCNT):c.5982C>G (p.Val1994=) rs552463011
NM_006031.6(PCNT):c.6080A>G (p.Gln2027Arg) rs147189224
NM_006031.6(PCNT):c.6125G>A (p.Arg2042His) rs149264703
NM_006031.6(PCNT):c.6150+3G>A rs760779996
NM_006031.6(PCNT):c.6277G>A (p.Asp2093Asn) rs200303861
NM_006031.6(PCNT):c.6634C>T (p.Arg2212Trp) rs144471022
NM_006031.6(PCNT):c.6933C>T (p.Val2311=) rs148444313
NM_006031.6(PCNT):c.7413G>A (p.Glu2471=) rs191561981
NM_006031.6(PCNT):c.7459C>G (p.Leu2487Val) rs201185279
NM_006031.6(PCNT):c.7495-13A>G rs114588443
NM_006031.6(PCNT):c.8224G>C (p.Glu2742Gln) rs35557109
NM_006031.6(PCNT):c.8671G>A (p.Ala2891Thr) rs33956783
NM_006031.6(PCNT):c.9279G>A (p.Ser3093=)
NM_006031.6(PCNT):c.9394-3T>C
NM_006031.6(PCNT):c.9707G>A (p.Arg3236Gln) rs113591604
NM_006031.6(PCNT):c.9949T>C (p.Leu3317=) rs111389121

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