Variant #0000569563 (NC_000020.10:g.3897560_3897565dup, NC_000020.10(NM_153638.2):c.1413-14_1413-9dup (PANK2))
| Chromosome |
20 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.3897560_3897565dup |
| DNA change (hg38) |
g.3916913_3916918dup |
| Published as |
PANK2(NM_001324191.2):c.540-14_540-9dupTTCCCC, PANK2(NM_153638.4):c.1413-14_1413-9dupTTCCCC, PANK2(NM_153638.4):c.1413-8delCinsTTCCCCC |
| ISCN |
- |
| DB-ID |
PANK2_000026 See all 2 reported entries |
| Variant remarks |
VKGL data sharing initiative Nederland |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
CLASSIFICATION record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
VKGL-NL_VUmc |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_VUmc |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2024-02-26 20:06:56 +01:00 (CET) |

Variant on transcripts
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