NM_000218.3(KCNQ1):c.1379G>A (p.Gly460Asp) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 16, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001773422.11
Allele description [Variation Report for NM_000218.3(KCNQ1):c.1379G>A (p.Gly460Asp)]
NM_000218.3(KCNQ1):c.1379G>A (p.Gly460Asp)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
602385903F1 NIH_MGC_93 Homo sapiens cDNA clone IMAGE:4514688 5', mRNA sequence
602385903F1 NIH_MGC_93 Homo sapiens cDNA clone IMAGE:4514688 5', mRNA sequencegi|13046974|gnl|dbEST|7929141|gb|BG 3.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Oct 13, 2024