ClinVar Genomic variation as it relates to human health
NM_015846.4(MBD1):c.751C>G (p.Leu251Val)
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.
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.
No data submitted for somatic clinical impact
No data submitted for oncogenicity
Variant Details
- Identifiers
-
NM_015846.4(MBD1):c.751C>G (p.Leu251Val)
Variation ID: 2597795 Accession: VCV002597795.2
- Type and length
-
single nucleotide variant, 1 bp
- Location
-
Cytogenetic: 18q21.1 18: 50275641 (GRCh38) [ NCBI UCSC ] 18: 47802011 (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
-
Nucleotide Protein Molecular
consequenceNM_015846.4:c.751C>G MANE Select Help Transcripts from the Matched Annotation from the NCBI and EMBL-EBI (MANE) collaboration.
NP_056671.2:p.Leu251Val missense NM_001204136.2:c.751C>G NP_001191065.1:p.Leu251Val missense NM_001204137.2:c.751C>G NP_001191066.1:p.Leu251Val missense NM_001204138.2:c.751C>G NP_001191067.1:p.Leu251Val missense NM_001204139.2:c.751C>G NP_001191068.1:p.Leu251Val missense NM_001204140.2:c.751C>G NP_001191069.1:p.Leu251Val missense NM_001204141.2:c.604C>G NP_001191070.1:p.Leu202Val missense NM_001204142.2:c.751C>G NP_001191071.1:p.Leu251Val missense NM_001204143.2:c.751C>G NP_001191072.1:p.Leu251Val missense NM_001204151.3:c.751C>G NP_001191080.1:p.Leu251Val missense NM_001323942.2:c.751C>G NP_001310871.1:p.Leu251Val missense NM_001323947.2:c.751C>G NP_001310876.1:p.Leu251Val missense NM_001323949.2:c.244C>G NP_001310878.1:p.Leu82Val missense NM_001323950.2:c.751C>G NP_001310879.1:p.Leu251Val missense NM_001323951.2:c.751C>G NP_001310880.1:p.Leu251Val missense NM_001323952.2:c.676C>G NP_001310881.1:p.Leu226Val missense NM_001323953.2:c.244C>G NP_001310882.1:p.Leu82Val missense NM_001323954.2:c.751C>G NP_001310883.1:p.Leu251Val missense NM_001388138.1:c.751C>G NP_001375067.1:p.Leu251Val missense NM_001388139.1:c.751C>G NP_001375068.1:p.Leu251Val missense NM_001388140.1:c.751C>G NP_001375069.1:p.Leu251Val missense NM_001388141.1:c.751C>G NP_001375070.1:p.Leu251Val missense NM_001388142.1:c.751C>G NP_001375071.1:p.Leu251Val missense NM_001388143.1:c.751C>G NP_001375072.1:p.Leu251Val missense NM_001388144.1:c.751C>G NP_001375073.1:p.Leu251Val missense NM_001388145.1:c.751C>G NP_001375074.1:p.Leu251Val missense NM_001388146.1:c.751C>G NP_001375075.1:p.Leu251Val missense NM_001388147.1:c.751C>G NP_001375076.1:p.Leu251Val missense NM_001388148.1:c.751C>G NP_001375077.1:p.Leu251Val missense NM_001388149.1:c.751C>G NP_001375078.1:p.Leu251Val missense NM_001388150.1:c.751C>G NP_001375079.1:p.Leu251Val missense NM_001388151.1:c.751C>G NP_001375080.1:p.Leu251Val missense NM_001388152.1:c.751C>G NP_001375081.1:p.Leu251Val missense NM_001388153.1:c.751C>G NP_001375082.1:p.Leu251Val missense NM_001388154.1:c.751C>G NP_001375083.1:p.Leu251Val missense NM_001388155.1:c.751C>G NP_001375084.1:p.Leu251Val missense NM_001388156.1:c.751C>G NP_001375085.1:p.Leu251Val missense NM_001388157.1:c.751C>G NP_001375086.1:p.Leu251Val missense NM_001388158.1:c.751C>G NP_001375087.1:p.Leu251Val missense NM_001388159.1:c.751C>G NP_001375088.1:p.Leu251Val missense NM_001388160.1:c.751C>G NP_001375089.1:p.Leu251Val missense NM_001388161.1:c.751C>G NP_001375090.1:p.Leu251Val missense NM_001388162.1:c.751C>G NP_001375091.1:p.Leu251Val missense NM_001388163.1:c.751C>G NP_001375092.1:p.Leu251Val missense NM_001388164.1:c.751C>G NP_001375093.1:p.Leu251Val missense NM_001388165.1:c.751C>G NP_001375094.1:p.Leu251Val missense NM_001388166.1:c.751C>G NP_001375095.1:p.Leu251Val missense NM_001388167.1:c.751C>G NP_001375096.1:p.Leu251Val missense NM_001399879.1:c.751C>G NP_001386808.1:p.Leu251Val missense NM_001399880.1:c.829C>G NP_001386809.1:p.Leu277Val missense NM_001399881.1:c.751C>G NP_001386810.1:p.Leu251Val missense NM_001399882.1:c.751C>G NP_001386811.1:p.Leu251Val missense NM_001399883.1:c.751C>G NP_001386812.1:p.Leu251Val missense NM_001399884.1:c.751C>G NP_001386813.1:p.Leu251Val missense NM_001399885.1:c.751C>G NP_001386814.1:p.Leu251Val missense NM_001399886.1:c.751C>G NP_001386815.1:p.Leu251Val missense NM_001399887.1:c.676C>G NP_001386816.1:p.Leu226Val missense NM_001399888.1:c.751C>G NP_001386817.1:p.Leu251Val missense NM_001399889.1:c.751C>G NP_001386818.1:p.Leu251Val missense NM_001399890.1:c.751C>G NP_001386819.1:p.Leu251Val missense NM_001399891.1:c.751C>G NP_001386820.1:p.Leu251Val missense NM_001399892.1:c.751C>G NP_001386821.1:p.Leu251Val missense NM_001399893.1:c.751C>G NP_001386822.1:p.Leu251Val missense NM_001399894.1:c.751C>G NP_001386823.1:p.Leu251Val missense NM_001399895.1:c.751C>G NP_001386824.1:p.Leu251Val missense NM_001399896.1:c.751C>G NP_001386825.1:p.Leu251Val missense NM_001399897.1:c.751C>G NP_001386826.1:p.Leu251Val missense NM_001399898.1:c.751C>G NP_001386827.1:p.Leu251Val missense NM_001399899.1:c.751C>G NP_001386828.1:p.Leu251Val missense NM_001399900.1:c.751C>G NP_001386829.1:p.Leu251Val missense NM_001399901.1:c.751C>G NP_001386830.1:p.Leu251Val missense NM_001399902.1:c.751C>G NP_001386831.1:p.Leu251Val missense NM_001399903.1:c.751C>G NP_001386832.1:p.Leu251Val missense NM_001399904.1:c.751C>G NP_001386833.1:p.Leu251Val missense NM_001399905.1:c.751C>G NP_001386834.1:p.Leu251Val missense NM_001399906.1:c.751C>G NP_001386835.1:p.Leu251Val missense NM_001399907.1:c.751C>G NP_001386836.1:p.Leu251Val missense NM_001399908.1:c.751C>G NP_001386837.1:p.Leu251Val missense NM_001399909.1:c.676C>G NP_001386838.1:p.Leu226Val missense NM_001399910.1:c.751C>G NP_001386839.1:p.Leu251Val missense NM_001399911.1:c.751C>G NP_001386840.1:p.Leu251Val missense NM_001399912.1:c.751C>G NP_001386841.1:p.Leu251Val missense NM_001399913.1:c.751C>G NP_001386842.1:p.Leu251Val missense NM_001399914.1:c.751C>G NP_001386843.1:p.Leu251Val missense NM_001399915.1:c.751C>G NP_001386844.1:p.Leu251Val missense NM_001399916.1:c.829C>G NP_001386845.1:p.Leu277Val missense NM_001399917.1:c.604C>G NP_001386846.1:p.Leu202Val missense NM_001399918.1:c.751C>G NP_001386847.1:p.Leu251Val missense NM_001399919.1:c.751C>G NP_001386848.1:p.Leu251Val missense NM_001399920.1:c.751C>G NP_001386849.1:p.Leu251Val missense NM_001399921.1:c.751C>G NP_001386850.1:p.Leu251Val missense NM_001399922.1:c.751C>G NP_001386851.1:p.Leu251Val missense NM_001399923.1:c.751C>G NP_001386852.1:p.Leu251Val missense NM_001399924.1:c.676C>G NP_001386853.1:p.Leu226Val missense NM_001399925.1:c.751C>G NP_001386854.1:p.Leu251Val missense NM_001399926.1:c.751C>G NP_001386855.1:p.Leu251Val missense NM_001399927.1:c.751C>G NP_001386856.1:p.Leu251Val missense NM_001399928.1:c.751C>G NP_001386857.1:p.Leu251Val missense NM_001399929.1:c.604C>G NP_001386858.1:p.Leu202Val missense NM_001399930.1:c.676C>G NP_001386859.1:p.Leu226Val missense NM_001399931.1:c.751C>G NP_001386860.1:p.Leu251Val missense NM_001399932.1:c.751C>G NP_001386861.1:p.Leu251Val missense NM_001399933.1:c.751C>G NP_001386862.1:p.Leu251Val missense NM_001399934.1:c.751C>G NP_001386863.1:p.Leu251Val missense NM_001399935.1:c.751C>G NP_001386864.1:p.Leu251Val missense NM_001399936.1:c.751C>G NP_001386865.1:p.Leu251Val missense NM_001399937.1:c.751C>G NP_001386866.1:p.Leu251Val missense NM_001399938.1:c.604C>G NP_001386867.1:p.Leu202Val missense NM_001399939.1:c.751C>G NP_001386868.1:p.Leu251Val missense NM_001399940.1:c.751C>G NP_001386869.1:p.Leu251Val missense NM_001399941.1:c.751C>G NP_001386870.1:p.Leu251Val missense NM_001399942.1:c.751C>G NP_001386871.1:p.Leu251Val missense NM_001399943.1:c.751C>G NP_001386872.1:p.Leu251Val missense NM_001399944.1:c.604C>G NP_001386873.1:p.Leu202Val missense NM_001399945.1:c.751C>G NP_001386874.1:p.Leu251Val missense NM_001399946.1:c.751C>G NP_001386875.1:p.Leu251Val missense NM_001399947.1:c.751C>G NP_001386876.1:p.Leu251Val missense NM_001399948.1:c.751C>G NP_001386877.1:p.Leu251Val missense NM_001399949.1:c.751C>G NP_001386878.1:p.Leu251Val missense NM_001399950.1:c.751C>G NP_001386879.1:p.Leu251Val missense NM_001399952.1:c.751C>G NP_001386881.1:p.Leu251Val missense NM_001399953.1:c.751C>G NP_001386882.1:p.Leu251Val missense NM_001399954.1:c.751C>G NP_001386883.1:p.Leu251Val missense NM_001399955.1:c.604C>G NP_001386884.1:p.Leu202Val missense NM_001399956.1:c.751C>G NP_001386885.1:p.Leu251Val missense NM_001399957.1:c.751C>G NP_001386886.1:p.Leu251Val missense NM_001399958.1:c.751C>G NP_001386887.1:p.Leu251Val missense NM_001399959.1:c.244C>G NP_001386888.1:p.Leu82Val missense NM_001399960.1:c.751C>G NP_001386889.1:p.Leu251Val missense NM_001399961.1:c.604C>G NP_001386890.1:p.Leu202Val missense NM_001399962.1:c.244C>G NP_001386891.1:p.Leu82Val missense NM_001399963.1:c.751C>G NP_001386892.1:p.Leu251Val missense NM_001399964.1:c.751C>G NP_001386893.1:p.Leu251Val missense NM_001399965.1:c.244C>G NP_001386894.1:p.Leu82Val missense NM_001399966.1:c.244C>G NP_001386895.1:p.Leu82Val missense NM_001399967.1:c.244C>G NP_001386896.1:p.Leu82Val missense NM_001399968.1:c.244C>G NP_001386897.1:p.Leu82Val missense NM_001399970.1:c.244C>G NP_001386899.1:p.Leu82Val missense NM_001399971.1:c.244C>G NP_001386900.1:p.Leu82Val missense NM_001399973.1:c.244C>G NP_001386902.1:p.Leu82Val missense NM_001399974.1:c.244C>G NP_001386903.1:p.Leu82Val missense NM_001399975.1:c.244C>G NP_001386904.1:p.Leu82Val missense NM_001399976.1:c.244C>G NP_001386905.1:p.Leu82Val missense NM_002384.3:c.751C>G NP_002375.1:p.Leu251Val missense NM_015844.3:c.751C>G NP_056669.2:p.Leu251Val missense NM_015845.4:c.751C>G NP_056670.2:p.Leu251Val missense NM_015847.4:c.604C>G NP_056723.2:p.Leu202Val missense NC_000018.10:g.50275641G>C NC_000018.9:g.47802011G>C NG_029505.1:g.11134C>G NG_138858.1:g.434G>C - Protein change
- L226V, L277V, L202V, L82V, L251V
- Other names
- -
- Canonical SPDI
- NC_000018.10:50275640:G: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. |
|||
MBD1 | - | - |
GRCh38 GRCh37 |
36 | 77 |
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 | RCV004345078.1 |
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
|
not specified
Affected status: unknown
Allele origin:
germline
|
Ambry Genetics
Accession: SCV004062770.2
First in ClinVar: Oct 28, 2023 Last updated: May 01, 2024 |
Comment:
The c.751C>G (p.L251V) alteration is located in exon 8 (coding exon 7) of the MBD1 gene. This alteration results from a C to G substitution … (more)
The c.751C>G (p.L251V) alteration is located in exon 8 (coding exon 7) of the MBD1 gene. This alteration results from a C to G substitution at nucleotide position 751, causing the leucine (L) at amino acid position 251 to be replaced by a valine (V). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear. (less)
|
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. |
Citations for germline classification of this variant
HelpThere 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 Jun 10, 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.