The c.3763G>A (p.G1255R) alteration is located in exon 30 (coding exon 30) of the SORBS1 gene. This alteration results from a G to A substitution at nucleotide position 3763, causing the glycine (G) at amino acid position 1255 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_001034954.3(SORBS1):c.3763G>A (p.Gly1255Arg)
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)
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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
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NM_001034954.3(SORBS1):c.3763G>A (p.Gly1255Arg)
Variation ID: 2411730 Accession: VCV002411730.2
- Type and length
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single nucleotide variant, 1 bp
- Location
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Cytogenetic: 10q24.1 10: 95318368 (GRCh38) [ NCBI UCSC ] 10: 97078125 (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 Feb 8, 2023 May 1, 2024 Dec 27, 2022 - HGVS
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... more HGVS ... less HGVSNucleotide Protein Molecular
consequenceNM_001034954.3:c.3763G>A MANE Select Help Transcripts from the Matched Annotation from the NCBI and EMBL-EBI (MANE) collaboration.
NP_001030126.2:p.Gly1255Arg missense NM_001034955.2:c.3340G>A NP_001030127.2:p.Gly1114Arg missense NM_001034956.2:c.2602G>A NP_001030128.2:p.Gly868Arg missense NM_001034957.3:c.2107G>A NP_001030129.2:p.Gly703Arg missense NM_001290294.2:c.3685G>A NP_001277223.2:p.Gly1229Arg missense NM_001290295.2:c.2134G>A NP_001277224.2:p.Gly712Arg missense NM_001290296.2:c.2899G>A NP_001277225.2:p.Gly967Arg missense NM_001290297.3:c.2320G>A NP_001277226.2:p.Gly774Arg missense NM_001290298.3:c.2425G>A NP_001277227.2:p.Gly809Arg missense NM_001377197.1:c.2731G>A NP_001364126.1:p.Gly911Arg missense NM_001377198.1:c.2662G>A NP_001364127.1:p.Gly888Arg missense NM_001377199.1:c.2599G>A NP_001364128.1:p.Gly867Arg missense NM_001377200.1:c.2587G>A NP_001364129.1:p.Gly863Arg missense NM_001377201.1:c.2572G>A NP_001364130.1:p.Gly858Arg missense NM_001377202.1:c.2476G>A NP_001364131.1:p.Gly826Arg missense NM_001377203.1:c.2389G>A NP_001364132.1:p.Gly797Arg missense NM_001377204.1:c.2386G>A NP_001364133.1:p.Gly796Arg missense NM_001377205.1:c.2362G>A NP_001364134.1:p.Gly788Arg missense NM_001377206.1:c.2314G>A NP_001364135.1:p.Gly772Arg missense NM_001377207.1:c.2293G>A NP_001364136.1:p.Gly765Arg missense NM_001377208.1:c.2221G>A NP_001364137.1:p.Gly741Arg missense NM_001377209.1:c.2218G>A NP_001364138.1:p.Gly740Arg missense NM_001384447.1:c.4705G>A NP_001371376.1:p.Gly1569Arg missense NM_001384448.1:c.4744G>A NP_001371377.1:p.Gly1582Arg missense NM_001384449.1:c.4639G>A NP_001371378.1:p.Gly1547Arg missense NM_001384450.1:c.4573G>A NP_001371379.1:p.Gly1525Arg missense NM_001384451.1:c.3799G>A NP_001371380.1:p.Gly1267Arg missense NM_001384452.1:c.4771G>A NP_001371381.1:p.Gly1591Arg missense NM_001384453.1:c.3865G>A NP_001371382.1:p.Gly1289Arg missense NM_001384454.1:c.3865G>A NP_001371383.1:p.Gly1289Arg missense NM_001384455.1:c.2320G>A NP_001371384.1:p.Gly774Arg missense NM_001384456.1:c.2320G>A NP_001371385.1:p.Gly774Arg missense NM_001384457.1:c.2320G>A NP_001371386.1:p.Gly774Arg missense NM_001384458.1:c.2590G>A NP_001371387.1:p.Gly864Arg missense NM_001384459.1:c.2581G>A NP_001371388.1:p.Gly861Arg missense NM_001384460.1:c.2518G>A NP_001371389.1:p.Gly840Arg missense NM_001384461.1:c.2422G>A NP_001371390.1:p.Gly808Arg missense NM_001384462.1:c.2395G>A NP_001371391.1:p.Gly799Arg missense NM_001384463.1:c.2191G>A NP_001371392.1:p.Gly731Arg missense NM_001384464.1:c.2179G>A NP_001371393.1:p.Gly727Arg missense NM_001384465.1:c.2386G>A NP_001371394.1:p.Gly796Arg missense NM_006434.4:c.1939G>A NP_006425.3:p.Gly647Arg missense NM_015385.4:c.2335G>A NP_056200.2:p.Gly779Arg missense NM_024991.3:c.2230G>A NP_079267.2:p.Gly744Arg missense NC_000010.11:g.95318368C>T NC_000010.10:g.97078125C>T NG_034041.1:g.248053G>A NG_034041.2:g.248003G>A - Protein change
- G1255R, G1267R, G1289R, G1582R, G727R, G741R, G858R, G861R, G867R, G888R, G1114R, G1229R, G1569R, G703R, G744R, G765R, G772R, G809R, G826R, G840R, G868R, G1525R, G1547R, G731R, G740R, G774R, G779R, G797R, G863R, G864R, G1591R, G647R, G712R, G788R, G796R, G799R, G808R, G911R, G967R
- Other names
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- Canonical SPDI
- NC_000010.11:95318367:C:T
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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 | ||
|---|---|---|---|---|---|---|
| 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. |
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| SORBS1 | - | - |
GRCh38 GRCh37 |
112 | 142 | |
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
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Dec 27, 2022 | RCV004245794.1 |
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. |
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Uncertain significance
(Dec 27, 2022)
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criteria provided, single submitter
Method: clinical testing
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not specified
Affected status: unknown
Allele origin:
germline
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Ambry Genetics
Accession: SCV003756480.2
First in ClinVar: Feb 07, 2023 Last updated: May 01, 2024 |
Comment:
The c.3763G>A (p.G1255R) alteration is located in exon 30 (coding exon 30) of the SORBS1 gene. This alteration results from a G to A substitution … (more)
The c.3763G>A (p.G1255R) alteration is located in exon 30 (coding exon 30) of the SORBS1 gene. This alteration results from a G to A substitution at nucleotide position 3763, causing the glycine (G) at amino acid position 1255 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.3763G>A (p.G1255R) alteration is located in exon 30 (coding exon 30) of the SORBS1 gene. This alteration results from a G to A substitution at nucleotide position 3763, causing the glycine (G) at amino acid position 1255 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 Nov 03, 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.