NM_018194.6(HHAT):c.997G>A (p.Gly333Arg) AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 12, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000973009.7
Allele description [Variation Report for NM_018194.6(HHAT):c.997G>A (p.Gly333Arg)]
NM_018194.6(HHAT):c.997G>A (p.Gly333Arg)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
TRA2B transformer 2 beta homolog [Homo sapiens]
TRA2B transformer 2 beta homolog [Homo sapiens]Gene ID:6434Gene
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Gene Links for GEO Profiles (Select 41463541) (1)
Gene
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Homo sapiens chromosome 19 genomic scaffold, GRCh38.p14 alternate locus group AL...
Homo sapiens chromosome 19 genomic scaffold, GRCh38.p14 alternate locus group ALT_REF_LOCI_6 HSCHR19LRC_LRC_T_CTG3_1gi|568815566|gnl|ASM:GCF_000001365. HR19LRC_LRC_T_CTG3_1|ref|NW_003571059.2||gpp|GPS_003206106.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: May 12, 2024