NM_017772.4(TBC1D22B):c.7G>T (p.Ala3Ser) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 27, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004160886.1
Allele description [Variation Report for NM_017772.4(TBC1D22B):c.7G>T (p.Ala3Ser)]
NM_017772.4(TBC1D22B):c.7G>T (p.Ala3Ser)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
PREDICTED: Homo sapiens Rho GTPase activating protein 33 (ARHGAP33), transcript ...
PREDICTED: Homo sapiens Rho GTPase activating protein 33 (ARHGAP33), transcript variant X1, mRNAgi|2462562733|ref|XM_054319717.1|Nucleotide
-
ERP013159 (46)
SRA
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Oct 13, 2024