NM_001387025.1(GRAMD1B):c.2109G>A (p.Thr703=) AND GRAMD1B-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 6, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003943210.2
Allele description [Variation Report for NM_001387025.1(GRAMD1B):c.2109G>A (p.Thr703=)]
NM_001387025.1(GRAMD1B):c.2109G>A (p.Thr703=)
Condition(s)
- Name:
- GRAMD1B-related disorder
- Synonyms:
- GRAMD1B-related condition
- Identifiers:
-
zx16b04.s1 Soares_total_fetus_Nb2HF8_9w Homo sapiens cDNA clone IMAGE:786607 3',...
zx16b04.s1 Soares_total_fetus_Nb2HF8_9w Homo sapiens cDNA clone IMAGE:786607 3', mRNA sequencegi|2207114|gnl|dbEST|1123593|gb|AA4 .1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Oct 13, 2024