Variant #0000529792 (NC_000006.11:g.7585967G>C, NM_004415.2:c.8472G>C (DSP))
| Chromosome |
6 |
| 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.7585967G>C |
| DNA change (hg38) |
g.7585734G>C |
| Published as |
DSP(NM_004415.2):c.8472G>C (p.G2824=), DSP(NM_004415.2):c.8472_8484delGTCCCGCTCCGGCinsCTCCCGCTCCGGC (p.G2824_G2828=), DSP(NM_004415.4):c.8472G>C ...) |
| ISCN |
- |
| DB-ID |
DSP_000086 See all 7 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) |
0.71375 View details |
| Owner |
VKGL-NL_Nijmegen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Nijmegen |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2025-05-05 21:14:00 +02:00 (CEST) |

Variant on transcripts
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