NM_022369.4(STRA6):c.1301-12C>T AND Matthew-Wood syndrome
- Germline classification:
- Benign/Likely benign (2 submissions)
- Last evaluated:
- Jan 14, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001117645.7
Allele description [Variation Report for NM_022369.4(STRA6):c.1301-12C>T]
NM_022369.4(STRA6):c.1301-12C>T
Condition(s)
- Name:
- Matthew-Wood syndrome (MCOPS9)
- Synonyms:
- ANOPHTHALMIA, CLINICAL, WITH MILD FACIAL DYSMORPHISM AND VARIABLE MALFORMATIONS OF THE LUNG, HEART, AND DIAPHRAGM; PULMONARY AGENESIS, MICROPHTHALMIA, AND DIAPHRAGMATIC DEFECT; Microphthalmia syndromic 9; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0011010; MedGen: C1832661; Orphanet: 2470; OMIM: 601186
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Homo sapiens cDNA FLJ35605 fis, clone SPLEN2009340
Homo sapiens cDNA FLJ35605 fis, clone SPLEN2009340gi|21751634|dbj|AK092924.1|Nucleotide
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EST198931 Normalized rat brain, Bento Soares Rattus sp. cDNA clone RBRAJ70 3' en...
EST198931 Normalized rat brain, Bento Soares Rattus sp. cDNA clone RBRAJ70 3' end, mRNA sequencegi|3103348|gnl|dbEST|1676724|gb|AA9 .1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024