ClinVar Genomic variation as it relates to human health
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- Interpretation:
-
Likely benign
- Review status:
- criteria provided, single submitter
- Submissions:
- 1
- First in ClinVar:
- Apr 8, 2022
- Most recent Submission:
- Apr 8, 2022
- Last evaluated:
- Aug 6, 2021
- Accession:
- VCV001663374.3
- Variation ID:
- 1663374
- Description:
- single nucleotide variant
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NM_001048174.2(MUTYH):c.704+13G>A
- Allele ID
- 1619683
- Variant type
- single nucleotide variant
- Variant length
- 1 bp
- Cytogenetic location
- 1p34.1
- Genomic location
- 1: 45332378 (GRCh38) GRCh38 UCSC
- 1: 45798050 (GRCh37) GRCh37 UCSC
- HGVS
- ... more HGVS ... less HGVS
- Protein change
- -
- Other names
- -
- Canonical SPDI
- NC_000001.11:45332377:C:T
- Functional consequence
- -
- Global minor allele frequency (GMAF)
- -
- Allele frequency
- -
- Links
- VarSome
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Aggregate interpretations per condition
| Interpreted condition | Interpretation | Number of submissions | Review status | Last evaluated | Variation/condition record |
|---|---|---|---|---|---|
| Likely benign | 1 | criteria provided, single submitter | Aug 6, 2021 | RCV002188471.3 |
Submitted interpretations and evidence
Help| Interpretation (Last evaluated) |
Review status (Assertion criteria) |
Condition (Inheritance) |
Submitter | More information | |
|---|---|---|---|---|---|
|
Likely benign
(Aug 06, 2021)
|
criteria provided, single submitter
Method: clinical testing
|
Familial adenomatous polyposis 2
Affected status: unknown
Allele origin:
germline
|
Invitae
Accession: SCV002484312.1
First in ClinVar: Apr 08, 2022 Last updated: Apr 08, 2022 |
|
Functional evidence
Help| 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 this variant
Help| There are no citations in ClinVar for this variation. If you know of citations for this variation, please consider submitting that information to ClinVar. |
Record last updated Nov 05, 2022