ClinVar Miner

Submissions for variant NM_003977.4(AIP):c.135C>T (p.Asp45=) (rs181969066)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000566236 SCV000672443 likely benign Hereditary cancer-predisposing syndrome 2017-07-05 criteria provided, single submitter clinical testing In silico models in agreement (benign);Synonymous alterations with insufficient evidence to classify as benign
Invitae RCV001444595 SCV001647604 likely benign not provided 2020-11-23 criteria provided, single submitter clinical testing
GeneReviews RCV000034061 SCV000057991 probable-non-pathogenic Somatotroph adenoma 2012-06-21 no assertion criteria provided curation Converted during submission to Likely benign.

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