Variant (CDS) | Variant (protein) | Variant Type | Variant Effect | Genomic Location (GRCh37) | ExAC Frequency |
c.1399G>A | p.E467K (Glu > Lys) | substitution | missense | chr10:69918324 (forward strand) | 0.01369693 |
As this variant is present at a population frequency of 0.01369693 (ExAC mean allelic frequency), it is highly unlikely to be pathogenic.
Database | European | African | East Asian | South Asian | American | Finnish | Other | Total |
---|---|---|---|---|---|---|---|---|
ExAC | 0.00039101 26 / 66494 | 0.14329738 1488 / 10384 | 0.00000000 0 / 8594 | 0.00030332 5 / 16484 | 0.01164610 134 / 11506 | 0.00000000 0 / 6608 | 0.00441501 4 / 906 | 0.01369693 1657 / 120976 |
ESP | 0.00070 6 / 8600 |
0.14435 636 / 4406 |
0.04936 642 / 13006 |
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1KG |
0.00000 0 / 1006 |
0.17625 233 / 1322 |
0.00000 0 / 1008 |
0.00000 0 / 978 |
0.01441 10 / 694 |
0.00000 0 / 198 |
0.04852 243 / 5008 |
0.00000 0 / 182 British |
0.13115 16 / 122 African-American |
0.00000 0 / 186 Chinese Dai |
0.00000 0 / 172 Bengali |
0.01064 2 / 188 Colombian |
||||
0.00000 0 / 214 Iberian |
0.15625 30 / 192 African-Caribbean |
0.00000 0 / 206 Han, Beijing |
0.00000 0 / 206 Gujarati Indian |
0.00781 1 / 128 Mexican, LA |
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0.00000 0 / 214 Toscani |
0.26263 52 / 198 Esan, Nigeria |
0.00000 0 / 208 Japanese |
0.00000 0 / 204 Indian Telugu |
0.00588 1 / 170 Peruvian |
||||
0.00000 0 / 198 Utah Europeans |
0.12832 29 / 226 Gambian |
0.00000 0 / 198 Kinh, Vietnam |
0.00000 0 / 192 Punjabi, Lahore |
0.02885 6 / 208 Puerto Rican |
||||
0.15152 30 / 198 Luhya, Kenya |
0.00000 0 / 210 Southern Han |
0.00000 0 / 204 Tamil |
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0.20000 34 / 170 Mende |
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0.19444 42 / 216 Yoruba, Nigeria |
The Exome Aggregation Consortium (ExAC) is a database of 60,706 unrelated individuals sequenced as part of various disease-specific and population genetic studies. There is partial overlap between ExAC and 1000 Genomes (1KG) (1,851 of the 2,504 samples in 1KG) and the Exome Sequencing Project (ESP) (3,936 of the 6,500 samples in ESP).
Canonical Sequences | ||||
---|---|---|---|---|
Transcript | ENST00000358913 | LRG_410t1 | NM_032578.2 | |
Protein | ENSP00000351790 | LRG_410p1 | Q86TC9 |
Missense Variant Predictions | ||||
---|---|---|---|---|
SIFT | Grantham | Polyphen-DIV | Polyphen-VAR | Summary 25% of algorithms have predicted that this variant will adversely affect protein function |
moderately conservative | possibly damaging | benign | ||
LRT | MutationTaster | MutationAssessor | FATHMM | |
neutral | disease-causing | neutral | tolerated |
1. Roddy Walsh, Kate L. Thomson, James S. Ware, Birgit H. Funke, Jessica Woodley, Karen J. McGuire, Francesco Mazzarotto, Edward Blair, Anneke Seller, Jenny C. Taylor, Eric V. Minikel, Exome Aggregation Consortium, Daniel G. MacArthur, Martin Farrall, Stuart A. Cook and Hugh Watkins. Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples. Genet Med. 2016 doi:10.1038/gim.2016.90.
2. Pugh TJ, Kelly MA, Gowrisankar S, Hynes E, Seidman MA, Baxter SM, Bowser M, Harrison B, Aaron D, Mahanta LM, Lakdawala NK, McDermott G, White ET, Rehm HL, Lebo M, Funke BH. The landscape of genetic variation in dilated cardiomyopathy as surveyed by clinical DNA sequencing. Genet Med. 2014 Aug;16(8):601-8.
3. Alfares AA, Kelly MA, McDermott G, Funke BH, Lebo MS, Baxter SB, Shen J, McLaughlin HM, Clark EH, Babb LJ, Cox SW, DePalma SR, Ho CY, Seidman JG, Seidman CE, Rehm HL.
Results of clinical genetic testing of 2,912 probands with hypertrophic cardiomyopathy: expanded panels offer limited additional sensitivity.
Genet Med. 2015 Nov;17(11):880-8.