ClinVar Miner

Submissions for variant NM_005157.6(ABL1):c.2350C>G (p.Pro784Ala)

gnomAD frequency: 0.00007  dbSNP: rs201376463
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ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002515810 SCV003275073 likely benign not provided 2024-10-23 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV002515810 SCV004156530 uncertain significance not provided 2023-01-01 criteria provided, single submitter clinical testing
ITMI RCV000119942 SCV000084072 not provided not specified 2013-09-19 no assertion provided reference population

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