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NM_182894.3(VSX2):c.599G>C (p.Arg200Pro) AND not provided

Germline classification:
Pathogenic (2 submissions)
Last evaluated:
Jan 5, 2023
Review status:
Somatic classification
of clinical impact:
None
Review status:
no assertion criteria provided
Somatic classification
of oncogenicity:
None
Review status:
no assertion criteria provided
Record status:
current
Accession:
RCV000413928.8

Allele description [Variation Report for NM_182894.3(VSX2):c.599G>C (p.Arg200Pro)]

NM_182894.3(VSX2):c.599G>C (p.Arg200Pro)

Gene:
VSX2:visual system homeobox 2 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
14q24.3
Genomic location:
Preferred name:
NM_182894.3(VSX2):c.599G>C (p.Arg200Pro)
HGVS:
  • NC_000014.9:g.74259621G>C
  • NG_013092.1:g.25150G>C
  • NM_182894.3:c.599G>CMANE SELECT
  • NP_878314.1:p.Arg200Pro
  • NC_000014.8:g.74726324G>C
  • NM_182894.2:c.599G>C
  • P58304:p.Arg200Pro
...more
Protein change:
R200P; ARG200PRO
Links:
UniProtKB: P58304#VAR_011618; OMIM: 142993.0002; dbSNP: rs121912543
NCBI 1000 Genomes Browser:
rs121912543
Molecular consequence:
  • NM_182894.3:c.599G>C - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:
none provided
Identifiers:
MedGen: C3661900

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV000491049GeneDx
criteria provided, single submitter

(GeneDx Variant Classification Process June 2021)
Pathogenic
(Aug 1, 2022)
germlineclinical testing

Citation Link,

SCV002020882Revvity Omics, Revvity
criteria provided, single submitter

(ACMG Guidelines, 2015)
Pathogenic
(Jan 5, 2023)
germlineclinical testing

PubMed (1)
[See all records that cite this PMID]

Last Updated: Oct 13, 2024

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