Variant #0000305313 (NC_000003.11:g.167422676C>T, NM_007217.3:c.104G>A (PDCD10))
| Chromosome |
3 |
| Allele |
Unknown |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.167422676C>T |
| DNA change (hg38) |
g.167704888C>T |
| Published as |
PDCD10(NM_007217.3):c.104G>A (p.R35Q, p.(Arg35Gln)), PDCD10(NM_007217.4):c.104G>A (p.R35Q), PDCD10(NM_145860.2):c.104G>A (p.R35Q) |
| ISCN |
- |
| DB-ID |
PDCD10_000010 See all 4 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) |
4.0E-5 View details |
| 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 |
2023-11-27 17:27:23 +01:00 (CET) |

Variant on transcripts
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