Variant #0000535199 (NC_000008.10:g.62580820_62580821insTGGGA, NC_000008.10(NM_004318.3):c.322+12706_322+12707insTCCCA (ASPH))
Chromosome |
8 |
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.62580820_62580821insTGGGA |
DNA change (hg38) |
g.61668261_61668262insTGGGA |
Published as |
ASPH(NM_020164.4):c.294_295insTCCCA (p.V99Sfs*3), ASPH(NM_020164.5):c.294_295insTCCCA (p.V99Sfs*3) |
ISCN |
- |
DB-ID |
ASPH_000034 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) |
0.00033 View details |
Owner |
VKGL-NL_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2019-12-04 15:24:38 +01:00 (CET) |

Variant on transcripts
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