The c.851A>G (p.Q284R) alteration is located in exon 8 (coding exon 7) of the HNRNPH1 gene. This alteration results from a A to G substitution at nucleotide position 851, causing the glutamine (Q) at amino acid position 284 to be replaced by an arginine (R). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear.
ClinVar Genomic variation as it relates to human health
NM_001257293.2(HNRNPH1):c.851A>G (p.Gln284Arg)
Germline
Classification
Help
The aggregate germline classification for this variant, typically for a monogenic or Mendelian disorder as in the ACMG/AMP guidelines, or for response to a drug. This value is calculated by NCBI based on data from submitters. Read our rules for calculating the aggregate classification.
(1)
Help
Stars represent the aggregate review status, or the level of review supporting the aggregate germline classification for this VCV record. This value is calculated by NCBI based on data from submitters. Read our rules for calculating the review status. The number of submissions which contribute to this review status is shown in parentheses.
Uncertain significance
1
criteria provided, single submitter
Somatic
No data submitted for somatic clinical impact
Somatic
No data submitted for oncogenicity
Variant Details
- Identifiers
-
NM_001257293.2(HNRNPH1):c.851A>G (p.Gln284Arg)
Variation ID: 2624213 Accession: VCV002624213.2
- Type and length
-
single nucleotide variant, 1 bp
- Location
-
Cytogenetic: 5q35.3 5: 179617869 (GRCh38) [ NCBI UCSC ] 5: 179044870 (GRCh37) [ NCBI UCSC ]
- Timeline in ClinVar
-
First in ClinVar Help The date this variant first appeared in ClinVar with each type of classification.
Last submission Help The date of the most recent submission for each type of classification for this variant.
Last evaluated Help The most recent date that a submitter evaluated this variant for each type of classification.
Germline Oct 28, 2023 May 1, 2024 Sep 14, 2023 - HGVS
-
... more HGVS ... less HGVSNucleotide Protein Molecular
consequenceNM_001257293.2:c.851A>G MANE Select Help Transcripts from the Matched Annotation from the NCBI and EMBL-EBI (MANE) collaboration.
NP_001244222.1:p.Gln284Arg missense NM_001363572.2:c.851A>G NP_001350501.1:p.Gln284Arg missense NM_001364225.2:c.851A>G NP_001351154.1:p.Gln284Arg missense NM_001364226.2:c.851A>G NP_001351155.1:p.Gln284Arg missense NM_001364227.2:c.851A>G NP_001351156.1:p.Gln284Arg missense NM_001364228.2:c.851A>G NP_001351157.1:p.Gln284Arg missense NM_001364229.2:c.851A>G NP_001351158.1:p.Gln284Arg missense NM_001364230.2:c.851A>G NP_001351159.1:p.Gln284Arg missense NM_001364231.2:c.851A>G NP_001351160.1:p.Gln284Arg missense NM_001364232.2:c.851A>G NP_001351161.1:p.Gln284Arg missense NM_001364233.2:c.851A>G NP_001351162.1:p.Gln284Arg missense NM_001364234.2:c.851A>G NP_001351163.1:p.Gln284Arg missense NM_001364235.2:c.851A>G NP_001351164.1:p.Gln284Arg missense NM_001364236.2:c.851A>G NP_001351165.1:p.Gln284Arg missense NM_001364237.2:c.851A>G NP_001351166.1:p.Gln284Arg missense NM_001364238.2:c.851A>G NP_001351167.1:p.Gln284Arg missense NM_001364239.2:c.851A>G NP_001351168.1:p.Gln284Arg missense NM_001364240.2:c.830A>G NP_001351169.1:p.Gln277Arg missense NM_001364241.2:c.830A>G NP_001351170.1:p.Gln277Arg missense NM_001364242.2:c.830A>G NP_001351171.1:p.Gln277Arg missense NM_001364243.2:c.830A>G NP_001351172.1:p.Gln277Arg missense NM_001364244.2:c.851A>G NP_001351173.1:p.Gln284Arg missense NM_001364245.2:c.851A>G NP_001351174.1:p.Gln284Arg missense NM_001364246.2:c.851A>G NP_001351175.1:p.Gln284Arg missense NM_001364247.2:c.851A>G NP_001351176.1:p.Gln284Arg missense NM_001364248.2:c.830A>G NP_001351177.1:p.Gln277Arg missense NM_001364250.2:c.695A>G NP_001351179.1:p.Gln232Arg missense NM_001364251.2:c.248A>G NP_001351180.1:p.Gln83Arg missense NM_001364252.2:c.248A>G NP_001351181.1:p.Gln83Arg missense NM_001364253.2:c.248A>G NP_001351182.1:p.Gln83Arg missense NM_001364254.2:c.248A>G NP_001351183.1:p.Gln83Arg missense NM_001364255.2:c.248A>G NP_001351184.1:p.Gln83Arg missense NM_001395176.1:c.851A>G NP_001382105.1:p.Gln284Arg missense NM_001395177.1:c.851A>G NP_001382106.1:p.Gln284Arg missense NM_001395178.1:c.851A>G NP_001382107.1:p.Gln284Arg missense NM_001395179.1:c.830A>G NP_001382108.1:p.Gln277Arg missense NM_001395180.1:c.830A>G NP_001382109.1:p.Gln277Arg missense NM_001395181.1:c.851A>G NP_001382110.1:p.Gln284Arg missense NM_001395182.1:c.851A>G NP_001382111.1:p.Gln284Arg missense NM_001395183.1:c.851A>G NP_001382112.1:p.Gln284Arg missense NM_001395184.1:c.851A>G NP_001382113.1:p.Gln284Arg missense NM_001395186.1:c.830A>G NP_001382115.1:p.Gln277Arg missense NM_001395187.1:c.851A>G NP_001382116.1:p.Gln284Arg missense NM_001395188.1:c.830A>G NP_001382117.1:p.Gln277Arg missense NM_001395189.1:c.851A>G NP_001382118.1:p.Gln284Arg missense NM_001395190.1:c.620A>G NP_001382119.1:p.Gln207Arg missense NM_001395191.1:c.533A>G NP_001382120.1:p.Gln178Arg missense NM_001395192.1:c.533A>G NP_001382121.1:p.Gln178Arg missense NM_001395193.1:c.440A>G NP_001382122.1:p.Gln147Arg missense NM_001395194.1:c.248A>G NP_001382123.1:p.Gln83Arg missense NM_001395195.1:c.248A>G NP_001382124.1:p.Gln83Arg missense NM_005520.3:c.851A>G NP_005511.1:p.Gln284Arg missense NC_000005.10:g.179617869T>C NC_000005.9:g.179044870T>C - Protein change
- Q178R, Q232R, Q147R, Q83R, Q207R, Q277R, Q284R
- Other names
- -
- Canonical SPDI
- NC_000005.10:179617868:T:C
-
Functional
consequence HelpThe effect of the variant on RNA or protein function, based on experimental evidence from submitters.
- -
-
Global minor allele
frequency (GMAF) HelpThe global minor allele frequency calculated by the 1000 Genomes Project. The minor allele at this location is indicated in parentheses and may be different from the allele represented by this VCV record.
- -
-
Allele frequency
Help
The frequency of the allele represented by this VCV record.
- -
- Links
Genes
| Gene | OMIM | ClinGen Gene Dosage Sensitivity Curation |
Variation Viewer
Help
Links to Variation Viewer, a genome browser to view variation data from NCBI databases. |
Related variants | ||
|---|---|---|---|---|---|---|
| HI score
Help
The haploinsufficiency score for the gene, curated by ClinGen’s Dosage Sensitivity Curation task team. |
TS score
Help
The triplosensitivity score for the gene, curated by ClinGen’s Dosage Sensitivity Curation task team. |
Within gene
Help
The number of variants in ClinVar that are contained within this gene, with a link to view the list of variants. |
All
Help
The number of variants in ClinVar for this gene, including smaller variants within the gene and larger CNVs that overlap or fully contain the gene. |
|||
| HNRNPH1 | - | - |
GRCh38 GRCh38 GRCh37 |
3 | 95 | |
| LOC128966623 | - | - | - | GRCh38 | - | 109 |
Conditions - Germline
| Condition
Help
The condition for this variant-condition (RCV) record in ClinVar. |
Classification
Help
The aggregate germline classification for this variant-condition (RCV) record in ClinVar. The number of submissions that contribute to this aggregate classification is shown in parentheses. (# of submissions) |
Review status
Help
The aggregate review status for this variant-condition (RCV) record in ClinVar. This value is calculated by NCBI based on data from submitters. Read our rules for calculating the review status. |
Last evaluated
Help
The most recent date that a submitter evaluated this variant for the condition. |
Variation/condition record
Help
The RCV accession number, with most recent version number, for the variant-condition record, with a link to the RCV web page. |
|---|---|---|---|---|
| Uncertain significance (1) |
criteria provided, single submitter
|
Sep 14, 2023 | RCV003385526.2 |
Submissions - Germline
| Classification
Help
The submitted germline classification for each SCV record. (Last evaluated) |
Review status
Help
Stars represent the review status, or the level of review supporting the submitted (SCV) record. This value is calculated by NCBI based on data from the submitter. Read our rules for calculating the review status. This column also includes a link to the submitter’s assertion criteria if provided, and the collection method. (Assertion criteria) |
Condition
Help
The condition for the classification, provided by the submitter for this submitted (SCV) record. This column also includes the affected status and allele origin of individuals observed with this variant. |
Submitter
Help
The submitting organization for this submitted (SCV) record. This column also includes the SCV accession and version number, the date this SCV first appeared in ClinVar, and the date that this SCV was last updated in ClinVar. |
More information
Help
This column includes more information supporting the classification, including citations, the comment on classification, and detailed evidence provided as observations of the variant by the submitter. |
|
|---|---|---|---|---|---|
|
Uncertain significance
(Sep 14, 2023)
|
criteria provided, single submitter
Method: clinical testing
|
Inborn genetic diseases
Affected status: unknown
Allele origin:
germline
|
Ambry Genetics
Accession: SCV004090330.2
First in ClinVar: Oct 28, 2023 Last updated: May 01, 2024 |
Comment:
The c.851A>G (p.Q284R) alteration is located in exon 8 (coding exon 7) of the HNRNPH1 gene. This alteration results from a A to G substitution … (more)
The c.851A>G (p.Q284R) alteration is located in exon 8 (coding exon 7) of the HNRNPH1 gene. This alteration results from a A to G substitution at nucleotide position 851, causing the glutamine (Q) at amino acid position 284 to be replaced by an arginine (R). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear. (less)
|
Comment:
Germline Functional Evidence
| There is no functional evidence in ClinVar for this variation. If you have generated functional data for this variation, please consider submitting that data to ClinVar. |
Comment:
The c.851A>G (p.Q284R) alteration is located in exon 8 (coding exon 7) of the HNRNPH1 gene. This alteration results from a A to G substitution at nucleotide position 851, causing the glutamine (Q) at amino acid position 284 to be replaced by an arginine (R). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear.
Citations for germline classification of this variant
Help| There are no citations for germline classification of this variant in ClinVar. If you know of citations for this variation, please consider submitting that information to ClinVar. |
Text-mined citations for this variant ...
HelpRecord last updated May 01, 2024
This date represents the last time this VCV record was updated. The update may be due to an update to one of the included submitted records (SCVs), or due to an update that ClinVar made to the variant such as adding HGVS expressions or a rs number. So this date may be different from the date of the “most recent submission” reported at the top of this page.