ClinVar Genomic variation as it relates to human health
NM_001395002.1(MAP4K4):c.2638G>A (p.Ala880Thr)
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
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NM_001395002.1(MAP4K4):c.2638G>A (p.Ala880Thr)
Variation ID: 2618975 Accession: VCV002618975.2
- Type and length
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single nucleotide variant, 1 bp
- Location
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Cytogenetic: 2q11.2 2: 101869796 (GRCh38) [ NCBI UCSC ] 2: 102486258 (GRCh37) [ NCBI UCSC ]
- Timeline in ClinVar
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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 Aug 15, 2023 - HGVS
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Nucleotide Protein Molecular
consequenceNM_001395002.1:c.2638G>A MANE Select Help Transcripts from the Matched Annotation from the NCBI and EMBL-EBI (MANE) collaboration.
NP_001381931.1:p.Ala880Thr missense NM_001242559.2:c.2395G>A NP_001229488.1:p.Ala799Thr missense NM_001242560.2:c.2383G>A NP_001229489.1:p.Ala795Thr missense NM_001384476.1:c.2473G>A NP_001371405.1:p.Ala825Thr missense NM_001384477.1:c.2470G>A NP_001371406.1:p.Ala824Thr missense NM_001384478.1:c.2152G>A NP_001371407.1:p.Ala718Thr missense NM_001384480.1:c.2152G>A NP_001371409.1:p.Ala718Thr missense NM_001384481.1:c.2398G>A NP_001371410.1:p.Ala800Thr missense NM_001384482.1:c.2143G>A NP_001371411.1:p.Ala715Thr missense NM_001384483.1:c.2233G>A NP_001371412.1:p.Ala745Thr missense NM_001384484.1:c.2476G>A NP_001371413.1:p.Ala826Thr missense NM_001384485.1:c.2476G>A NP_001371414.1:p.Ala826Thr missense NM_001384486.1:c.2407G>A NP_001371415.1:p.Ala803Thr missense NM_001384487.1:c.2374G>A NP_001371416.1:p.Ala792Thr missense NM_001384488.1:c.2404G>A NP_001371417.1:p.Ala802Thr missense NM_001384489.1:c.1654G>A NP_001371418.1:p.Ala552Thr missense NM_001384490.1:c.2245G>A NP_001371419.1:p.Ala749Thr missense NM_001384491.1:c.2380G>A NP_001371420.1:p.Ala794Thr missense NM_001384492.1:c.2542G>A NP_001371421.1:p.Ala848Thr missense NM_001384493.1:c.2476G>A NP_001371422.1:p.Ala826Thr missense NM_001384494.1:c.2242G>A NP_001371423.1:p.Ala748Thr missense NM_001384495.1:c.2152G>A NP_001371424.1:p.Ala718Thr missense NM_001384496.1:c.2236G>A NP_001371425.1:p.Ala746Thr missense NM_001384497.1:c.2629G>A NP_001371426.1:p.Ala877Thr missense NM_001384505.1:c.1114G>A NP_001371434.1:p.Ala372Thr missense NM_001384506.1:c.2638G>A NP_001371435.1:p.Ala880Thr missense NM_001384507.1:c.2407G>A NP_001371436.1:p.Ala803Thr missense NM_001384508.1:c.2470G>A NP_001371437.1:p.Ala824Thr missense NM_001384509.1:c.2371G>A NP_001371438.1:p.Ala791Thr missense NM_001384520.1:c.2536G>A NP_001371449.1:p.Ala846Thr missense NM_001384543.1:c.2545G>A NP_001371472.1:p.Ala849Thr missense NM_001384544.1:c.1561G>A NP_001371473.1:p.Ala521Thr missense NM_001384545.1:c.1561G>A NP_001371474.1:p.Ala521Thr missense NM_001384548.1:c.2389G>A NP_001371477.1:p.Ala797Thr missense NM_001384549.1:c.2125G>A NP_001371478.1:p.Ala709Thr missense NM_001384550.1:c.2362G>A NP_001371479.1:p.Ala788Thr missense NM_001384551.1:c.2287G>A NP_001371480.1:p.Ala763Thr missense NM_001384552.1:c.2446G>A NP_001371481.1:p.Ala816Thr missense NM_001384553.1:c.2443G>A NP_001371482.1:p.Ala815Thr missense NM_001384554.1:c.2347G>A NP_001371483.1:p.Ala783Thr missense NM_001384555.1:c.2449G>A NP_001371484.1:p.Ala817Thr missense NM_001384556.1:c.2440G>A NP_001371485.1:p.Ala814Thr missense NM_001384557.1:c.2278G>A NP_001371486.1:p.Ala760Thr missense NM_001384558.1:c.2356G>A NP_001371487.1:p.Ala786Thr missense NM_001384559.1:c.2122G>A NP_001371488.1:p.Ala708Thr missense NM_001384560.1:c.2209G>A NP_001371489.1:p.Ala737Thr missense NM_001384561.1:c.2125G>A NP_001371490.1:p.Ala709Thr missense NM_001384562.1:c.2443G>A NP_001371491.1:p.Ala815Thr missense NM_001384563.1:c.2440G>A NP_001371492.1:p.Ala814Thr missense NM_001384564.1:c.2509G>A NP_001371493.1:p.Ala837Thr missense NM_001384567.1:c.2356G>A NP_001371496.1:p.Ala786Thr missense NM_001384572.1:c.2449G>A NP_001371501.1:p.Ala817Thr missense NM_001384579.1:c.2380G>A NP_001371508.1:p.Ala794Thr missense NM_004834.5:c.2149G>A NP_004825.3:p.Ala717Thr missense NM_145686.4:c.2305G>A NP_663719.2:p.Ala769Thr missense NM_145687.4:c.2314G>A NP_663720.1:p.Ala772Thr missense NR_169279.1:n.2771G>A non-coding transcript variant NR_169280.1:n.2678G>A non-coding transcript variant NR_169281.1:n.2678G>A non-coding transcript variant NR_169282.1:n.2231G>A non-coding transcript variant NC_000002.12:g.101869796G>A NC_000002.11:g.102486258G>A NG_076990.1:g.270G>A - Protein change
- A737T, A746T, A749T, A783T, A791T, A795T, A797T, A799T, A802T, A817T, A825T, A846T, A848T, A877T, A552T, A718T, A745T, A769T, A786T, A803T, A815T, A849T, A880T, A372T, A521T, A715T, A760T, A763T, A772T, A816T, A826T, A708T, A709T, A717T, A748T, A788T, A792T, A794T, A800T, A814T, A824T, A837T
- Other names
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- Canonical SPDI
- NC_000002.12:101869795:G:A
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Functional
consequence HelpThe effect of the variant on RNA or protein function, based on experimental evidence from submitters.
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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.
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Allele frequency
Help
The frequency of the allele represented by this VCV record.
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- 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 | ||
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HI score
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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. |
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LOC122817718 | - | - | - | GRCh38 | - | 14 |
MAP4K4 | - | - |
GRCh38 GRCh37 |
102 | - |
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
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The RCV accession number, with most recent version number, for the variant-condition record, with a link to the RCV web page. |
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Uncertain significance (1) |
criteria provided, single submitter
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Aug 15, 2023 | RCV003376972.2 |
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. |
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Uncertain significance
(Aug 15, 2023)
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criteria provided, single submitter
Method: clinical testing
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Inborn genetic diseases
Affected status: unknown
Allele origin:
germline
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Ambry Genetics
Accession: SCV004095545.2
First in ClinVar: Oct 28, 2023 Last updated: May 01, 2024 |
Comment:
The c.2305G>A (p.A769T) alteration is located in exon 20 (coding exon 20) of the MAP4K4 gene. This alteration results from a G to A substitution … (more)
The c.2305G>A (p.A769T) alteration is located in exon 20 (coding exon 20) of the MAP4K4 gene. This alteration results from a G to A substitution at nucleotide position 2305, causing the alanine (A) at amino acid position 769 to be replaced by a threonine (T). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear. (less)
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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 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.