NM_000545.8(HNF1A):c.955+94T>G AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jun 14, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000836328.1
Allele description [Variation Report for NM_000545.8(HNF1A):c.955+94T>G]
NM_000545.8(HNF1A):c.955+94T>G
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
H.sapiens EMX2 mRNA
H.sapiens EMX2 mRNAgi|31141|emb|X68880.1|Nucleotide
-
PRJNA1136665 (24)
SRA
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Dec 24, 2023