Variant #0000621926 (NC_000007.13:g.80303298G>A, NC_000007.13(NM_001001547.2):c.1255-1G>A (CD36))
Chromosome |
7 |
Allele |
Unknown |
Affects function (as reported) |
Probably affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
likely pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.80303298G>A |
DNA change (hg38) |
g.80673982G>A |
Published as |
CD36(NM_001001548.2):c.1255-1G>A |
ISCN |
- |
DB-ID |
CD36_000018 |
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) |
3.0E-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 |
2019-12-06 12:43:26 +01:00 (CET) |
Date last edited |
2020-06-23 09:58:36 +02:00 (CEST) |

Variant on transcripts
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