ClinVar Miner

Submissions for variant NM_005157.6(ABL1):c.2930G>A (p.Ser977Asn)

gnomAD frequency: 0.00001  dbSNP: rs587778015
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003764832 SCV004665494 likely benign not provided 2023-05-11 criteria provided, single submitter clinical testing
ITMI RCV000119951 SCV000084081 not provided not specified 2013-09-19 no assertion provided reference population

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