The c.1073T>C (p.I358T) alteration is located in exon 12 (coding exon 11) of the PTK2 gene. This alteration results from a T to C substitution at nucleotide position 1073, causing the isoleucine (I) at amino acid position 358 to be replaced by a threonine (T). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear.
ClinVar Genomic variation as it relates to human health
NM_001352702.2(PTK2):c.1007T>C (p.Ile336Thr)
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_001352702.2(PTK2):c.1007T>C (p.Ile336Thr)
Variation ID: 2402091 Accession: VCV002402091.2
- Type and length
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single nucleotide variant, 1 bp
- Location
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Cytogenetic: 8q24.3 8: 140800545 (GRCh38) [ NCBI UCSC ] 8: 141810644 (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 Apr 7, 2022 - HGVS
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... more HGVS ... less HGVSNucleotide Protein Molecular
consequenceNM_001352702.2:c.1007T>C MANE Select Help Transcripts from the Matched Annotation from the NCBI and EMBL-EBI (MANE) collaboration.
NP_001339631.1:p.Ile336Thr missense NM_001199649.2:c.1007T>C NP_001186578.1:p.Ile336Thr missense NM_001316342.2:c.668T>C NP_001303271.1:p.Ile223Thr missense NM_001352694.2:c.1007T>C NP_001339623.1:p.Ile336Thr missense NM_001352695.2:c.1007T>C NP_001339624.1:p.Ile336Thr missense NM_001352696.2:c.668T>C NP_001339625.1:p.Ile223Thr missense NM_001352697.2:c.1139T>C NP_001339626.1:p.Ile380Thr missense NM_001352698.2:c.1046T>C NP_001339627.1:p.Ile349Thr missense NM_001352699.2:c.1007T>C NP_001339628.1:p.Ile336Thr missense NM_001352700.2:c.1007T>C NP_001339629.1:p.Ile336Thr missense NM_001352701.2:c.1007T>C NP_001339630.1:p.Ile336Thr missense NM_001352703.2:c.1007T>C NP_001339632.1:p.Ile336Thr missense NM_001352704.2:c.1007T>C NP_001339633.1:p.Ile336Thr missense NM_001352705.2:c.1046T>C NP_001339634.1:p.Ile349Thr missense NM_001352706.2:c.1007T>C NP_001339635.1:p.Ile336Thr missense NM_001352707.2:c.1007T>C NP_001339636.1:p.Ile336Thr missense NM_001352708.2:c.1007T>C NP_001339637.1:p.Ile336Thr missense NM_001352709.2:c.1007T>C NP_001339638.1:p.Ile336Thr missense NM_001352710.2:c.1007T>C NP_001339639.1:p.Ile336Thr missense NM_001352711.2:c.1007T>C NP_001339640.1:p.Ile336Thr missense NM_001352712.2:c.1007T>C NP_001339641.1:p.Ile336Thr missense NM_001352713.2:c.1007T>C NP_001339642.1:p.Ile336Thr missense NM_001352714.2:c.1007T>C NP_001339643.1:p.Ile336Thr missense NM_001352715.2:c.1007T>C NP_001339644.1:p.Ile336Thr missense NM_001352716.2:c.899T>C NP_001339645.1:p.Ile300Thr missense NM_001352717.2:c.1007T>C NP_001339646.1:p.Ile336Thr missense NM_001352718.2:c.1007T>C NP_001339647.1:p.Ile336Thr missense NM_001352719.2:c.1007T>C NP_001339648.1:p.Ile336Thr missense NM_001352720.2:c.1007T>C NP_001339649.1:p.Ile336Thr missense NM_001352721.2:c.1007T>C NP_001339650.1:p.Ile336Thr missense NM_001352722.2:c.1007T>C NP_001339651.1:p.Ile336Thr missense NM_001352723.2:c.1007T>C NP_001339652.1:p.Ile336Thr missense NM_001352724.2:c.1007T>C NP_001339653.1:p.Ile336Thr missense NM_001352725.2:c.1007T>C NP_001339654.1:p.Ile336Thr missense NM_001352726.2:c.899T>C NP_001339655.1:p.Ile300Thr missense NM_001352727.2:c.1007T>C NP_001339656.1:p.Ile336Thr missense NM_001352728.2:c.899T>C NP_001339657.1:p.Ile300Thr missense NM_001352729.2:c.899T>C NP_001339658.1:p.Ile300Thr missense NM_001352730.2:c.668T>C NP_001339659.1:p.Ile223Thr missense NM_001352731.2:c.668T>C NP_001339660.1:p.Ile223Thr missense NM_001352732.2:c.668T>C NP_001339661.1:p.Ile223Thr missense NM_001352733.2:c.668T>C NP_001339662.1:p.Ile223Thr missense NM_001352734.2:c.668T>C NP_001339663.1:p.Ile223Thr missense NM_001352735.2:c.605T>C NP_001339664.1:p.Ile202Thr missense NM_001352736.2:c.704T>C NP_001339665.1:p.Ile235Thr missense NM_001352737.2:c.668T>C NP_001339666.1:p.Ile223Thr missense NM_001352738.2:c.668T>C NP_001339667.1:p.Ile223Thr missense NM_001352739.2:c.668T>C NP_001339668.1:p.Ile223Thr missense NM_001352740.2:c.668T>C NP_001339669.1:p.Ile223Thr missense NM_001352741.2:c.668T>C NP_001339670.1:p.Ile223Thr missense NM_001352742.2:c.605T>C NP_001339671.1:p.Ile202Thr missense NM_001352743.2:c.668T>C NP_001339672.1:p.Ile223Thr missense NM_001352744.2:c.560T>C NP_001339673.1:p.Ile187Thr missense NM_001352745.2:c.560T>C NP_001339674.1:p.Ile187Thr missense NM_001352746.2:c.497T>C NP_001339675.1:p.Ile166Thr missense NM_001352747.2:c.-633T>C 5 prime UTR NM_001352748.2:c.1007T>C NP_001339677.1:p.Ile336Thr missense NM_001387584.1:c.668T>C NP_001374513.1:p.Ile223Thr missense NM_001387585.1:c.1007T>C NP_001374514.1:p.Ile336Thr missense NM_001387586.1:c.1007T>C NP_001374515.1:p.Ile336Thr missense NM_001387587.1:c.1007T>C NP_001374516.1:p.Ile336Thr missense NM_001387590.1:c.560T>C NP_001374519.1:p.Ile187Thr missense NM_001387591.1:c.668T>C NP_001374520.1:p.Ile223Thr missense NM_001387592.1:c.65T>C NP_001374521.1:p.Ile22Thr missense NM_001387603.1:c.668T>C NP_001374532.1:p.Ile223Thr missense NM_001387604.1:c.65T>C NP_001374533.1:p.Ile22Thr missense NM_001387605.1:c.668T>C NP_001374534.1:p.Ile223Thr missense NM_001387606.1:c.668T>C NP_001374535.1:p.Ile223Thr missense NM_001387607.1:c.668T>C NP_001374536.1:p.Ile223Thr missense NM_001387608.1:c.668T>C NP_001374537.1:p.Ile223Thr missense NM_001387609.1:c.668T>C NP_001374538.1:p.Ile223Thr missense NM_001387610.1:c.485T>C NP_001374539.1:p.Ile162Thr missense NM_001387611.1:c.668T>C NP_001374540.1:p.Ile223Thr missense NM_001387612.1:c.668T>C NP_001374541.1:p.Ile223Thr missense NM_001387613.1:c.668T>C NP_001374542.1:p.Ile223Thr missense NM_001387614.1:c.1007T>C NP_001374543.1:p.Ile336Thr missense NM_001387615.1:c.899T>C NP_001374544.1:p.Ile300Thr missense NM_001387616.1:c.65T>C NP_001374545.1:p.Ile22Thr missense NM_001387617.1:c.65T>C NP_001374546.1:p.Ile22Thr missense NM_001387618.1:c.668T>C NP_001374547.1:p.Ile223Thr missense NM_001387619.1:c.899T>C NP_001374548.1:p.Ile300Thr missense NM_001387620.1:c.668T>C NP_001374549.1:p.Ile223Thr missense NM_001387621.1:c.65T>C NP_001374550.1:p.Ile22Thr missense NM_001387622.1:c.1007T>C NP_001374551.1:p.Ile336Thr missense NM_001387623.1:c.668T>C NP_001374552.1:p.Ile223Thr missense NM_001387624.1:c.899T>C NP_001374553.1:p.Ile300Thr missense NM_001387625.1:c.1007T>C NP_001374554.1:p.Ile336Thr missense NM_001387627.1:c.1007T>C NP_001374556.1:p.Ile336Thr missense NM_001387628.1:c.1007T>C NP_001374557.1:p.Ile336Thr missense NM_001387629.1:c.65T>C NP_001374558.1:p.Ile22Thr missense NM_001387630.1:c.485T>C NP_001374559.1:p.Ile162Thr missense NM_001387631.1:c.899T>C NP_001374560.1:p.Ile300Thr missense NM_001387632.1:c.1007T>C NP_001374561.1:p.Ile336Thr missense NM_001387633.1:c.1007T>C NP_001374562.1:p.Ile336Thr missense NM_001387634.1:c.1007T>C NP_001374563.1:p.Ile336Thr missense NM_001387635.1:c.560T>C NP_001374564.1:p.Ile187Thr missense NM_001387636.1:c.1007T>C NP_001374565.1:p.Ile336Thr missense NM_001387637.1:c.1007T>C NP_001374566.1:p.Ile336Thr missense NM_001387638.1:c.1007T>C NP_001374567.1:p.Ile336Thr missense NM_001387639.1:c.1007T>C NP_001374568.1:p.Ile336Thr missense NM_001387640.1:c.1007T>C NP_001374569.1:p.Ile336Thr missense NM_001387641.1:c.1046T>C NP_001374570.1:p.Ile349Thr missense NM_001387642.1:c.1007T>C NP_001374571.1:p.Ile336Thr missense NM_001387643.1:c.1139T>C NP_001374572.1:p.Ile380Thr missense NM_001387644.1:c.1046T>C NP_001374573.1:p.Ile349Thr missense NM_001387645.1:c.1007T>C NP_001374574.1:p.Ile336Thr missense NM_001387646.1:c.1139T>C NP_001374575.1:p.Ile380Thr missense NM_001387647.1:c.1007T>C NP_001374576.1:p.Ile336Thr missense NM_001387648.1:c.1139T>C NP_001374577.1:p.Ile380Thr missense NM_001387649.1:c.1139T>C NP_001374578.1:p.Ile380Thr missense NM_001387650.1:c.1139T>C NP_001374579.1:p.Ile380Thr missense NM_001387652.1:c.668T>C NP_001374581.1:p.Ile223Thr missense NM_001387653.1:c.899T>C NP_001374582.1:p.Ile300Thr missense NM_001387654.1:c.668T>C NP_001374583.1:p.Ile223Thr missense NM_001387655.1:c.1007T>C NP_001374584.1:p.Ile336Thr missense NM_001387656.1:c.1007T>C NP_001374585.1:p.Ile336Thr missense NM_001387657.1:c.1007T>C NP_001374586.1:p.Ile336Thr missense NM_001387658.1:c.1007T>C NP_001374587.1:p.Ile336Thr missense NM_001387659.1:c.1007T>C NP_001374588.1:p.Ile336Thr missense NM_001387660.1:c.1139T>C NP_001374589.1:p.Ile380Thr missense NM_001387661.1:c.1139T>C NP_001374590.1:p.Ile380Thr missense NM_001387662.1:c.1139T>C NP_001374591.1:p.Ile380Thr missense NM_005607.5:c.1073T>C NP_005598.3:p.Ile358Thr missense NM_153831.4:c.1007T>C NP_722560.1:p.Ile336Thr missense NR_148036.2:n.1286T>C non-coding transcript variant NR_148037.2:n.1401T>C non-coding transcript variant NR_148038.2:n.1119T>C non-coding transcript variant NR_148039.2:n.1011T>C non-coding transcript variant NR_170671.1:n.1030T>C non-coding transcript variant NR_170672.1:n.1197T>C non-coding transcript variant NR_170673.1:n.1197T>C non-coding transcript variant NC_000008.11:g.140800545A>G NC_000008.10:g.141810644A>G NG_029467.2:g.205769T>C - Protein change
- I300T, I349T, I358T, I166T, I223T, I22T, I235T, I380T, I162T, I187T, I202T, I336T
- Other names
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- Canonical SPDI
- NC_000008.11:140800544:A:G
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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
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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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| PTK2 | - | - |
GRCh38 GRCh37 |
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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
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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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Apr 7, 2022 | RCV004238952.1 |
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
(Apr 07, 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: SCV003753534.2
First in ClinVar: Feb 07, 2023 Last updated: May 01, 2024 |
Comment:
The c.1073T>C (p.I358T) alteration is located in exon 12 (coding exon 11) of the PTK2 gene. This alteration results from a T to C substitution … (more)
The c.1073T>C (p.I358T) alteration is located in exon 12 (coding exon 11) of the PTK2 gene. This alteration results from a T to C substitution at nucleotide position 1073, causing the isoleucine (I) at amino acid position 358 to be replaced by a threonine (T). 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.1073T>C (p.I358T) alteration is located in exon 12 (coding exon 11) of the PTK2 gene. This alteration results from a T to C substitution at nucleotide position 1073, causing the isoleucine (I) at amino acid position 358 to be replaced by a threonine (T). 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.