Variant #0000532199 (NC_000007.13:g.48390325C>T, NM_152701.3:c.10290C>T (ABCA13))
Chromosome |
7 |
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.48390325C>T |
DNA change (hg38) |
g.48350728C>T |
Published as |
ABCA13(NM_152701.4):c.10290C>T (p.C3430=) |
ISCN |
- |
DB-ID |
ABCA13_000046 |
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) |
0.00024 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 |
2020-06-22 16:06:55 +02:00 (CEST) |

Variant on transcripts
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