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NM_001007792.1(NTRK1):c.702G>A (p.Thr234=)

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Interpretation:
Likely benign​

Review status:
criteria provided, single submitter
Submissions:
3 (Most recent: Jan 7, 2021)
Last evaluated:
Aug 28, 2018
Accession:
VCV000772550.3
Variation ID:
772550
Description:
single nucleotide variant
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NM_001007792.1(NTRK1):c.702G>A (p.Thr234=)

Allele ID
696163
Variant type
single nucleotide variant
Variant length
1 bp
Cytogenetic location
1q23.1
Genomic location
1: 156871697 (GRCh38) GRCh38 UCSC
1: 156841489 (GRCh37) GRCh37 UCSC
HGVS
Nucleotide Protein Molecular
consequence
NC_000001.10:g.156841489G>A
NC_000001.11:g.156871697G>A
NM_001007792.1:c.702G>A NP_001007793.1:p.Thr234= synonymous
... more HGVS
Protein change
-
Other names
-
Canonical SPDI
NC_000001.11:156871696:G:A
Functional consequence
-
Global minor allele frequency (GMAF)
0.00020 (A)

Allele frequency
1000 Genomes Project 0.00020
Exome Aggregation Consortium (ExAC) 0.00001
Links
dbSNP: rs201110800
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 28, 2018 RCV000952133.1
Likely benign 2 criteria provided, single submitter Aug 27, 2018 RCV001274806.2
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Gene OMIM ClinGen Gene Dosage Sensitivity Curation Variation viewer Related variants
HI score Help TS score Help Within gene All
NTRK1 - - GRCh38
GRCh37
677 723

Submitted interpretations and evidence

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Interpretation
(Last evaluated)
Review status
(Assertion criteria)
Condition
(Inheritance)
Submitter Supporting information
Likely benign
(Aug 28, 2018)
criteria provided, single submitter
Method: clinical testing
not provided
Allele origin: germline
Invitae
Accession: SCV001098608.1
Submitted: (Mar 14, 2019)
Evidence details
Likely benign
(Aug 27, 2018)
criteria provided, single submitter
Method: clinical testing
Hereditary insensitivity to pain with anhidrosis
Allele origin: germline
Invitae
Accession: SCV001608345.1
Submitted: (Jan 07, 2021)
Evidence details
Likely benign
(Apr 17, 2020)
no assertion criteria provided
Method: clinical testing
Hereditary insensitivity to pain with anhidrosis
Allele origin: germline
Natera, Inc.
Accession: SCV001459286.1
Submitted: (Dec 28, 2020)
Evidence details

Functional evidence

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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

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There are no citations in ClinVar for this variation. If you know of citations for this variation, please consider submitting that information to ClinVar.

Text-mined citations for rs201110800...

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These citations are identified by LitVar using the rs number, so they may include citations for more than one variant at this location. Please review the LitVar results carefully for your variant of interest.

Record last updated Aug 27, 2021