ClinVar Miner

Submissions for variant NM_004448.4(ERBB2):c.3289G>A (p.Gly1097Arg)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV004907554 SCV005579127 uncertain significance not specified 2024-09-26 criteria provided, single submitter clinical testing The c.3289G>A (p.G1097R) alteration is located in exon 26 (coding exon 26) of the ERBB2 gene. This alteration results from a G to A substitution at nucleotide position 3289, causing the glycine (G) at amino acid position 1097 to be replaced by an arginine (R). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear.

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