Variant #0000530263 (NC_000007.13:g.103292201G>A, NM_005045.3:c.1799C>T (RELN))
Chromosome |
7 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
VUS |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.103292201G>A |
DNA change (hg38) |
g.103651754G>A |
Published as |
RELN(NM_005045.3):c.1799C>T (p.(Ser600Phe)), RELN(NM_005045.4):c.1799C>T (p.S600F), RELN(NM_173054.2):c.1799C>T (p.S600F) |
ISCN |
- |
DB-ID |
RELN_000247 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) |
0.01068 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 |
2023-01-11 15:44:22 +01:00 (CET) |

Variant on transcripts
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