Variant #0000139990 (NC_000019.9:g.6361955A>G, NC_000019.9(NM_006012.2):c.270+1G>A (CLPP))
| Chromosome |
19 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.6361955A>G |
| DNA change (hg38) |
g.6361944A>G |
| Published as |
- |
| ISCN |
- |
| DB-ID |
CLPP_000009 See all 4 reported entries |
| Variant remarks |
in vitro COS7 cell expression cloning; 23/37 clones normal splicing, 11/37 retained intron 2, 3/37 other aberrant transcripts Variant Error [EMISMATCH]: This variant seems to mismatch; the genomic and the transcript variant seems to not belong together. Please fix this entry and then remove this message. |
| Reference |
PubMed: Jenkinson 2013, Journal: Jenkinson 2013 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2016-11-10 10:53:41 +01:00 (CET) |
| Date last edited |
2020-07-14 21:50:58 +02:00 (CEST) |

Variant on transcripts
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