Variant #0000275400 (NC_000001.10:g.65830312_65830313del, NC_000001.10(NM_001256864.1):c.194-6_194-5del (DNAJC6))
| Chromosome |
1 |
| 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.65830312_65830313del |
| DNA change (hg38) |
g.65364629_65364630del |
| Published as |
DNAJC6(NM_001256864.2):c.194-6_194-5delTG |
| ISCN |
- |
| DB-ID |
DNAJC6_000005 |
| 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_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2020-06-04 16:08:04 +02:00 (CEST) |

Variant on transcripts
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