Variant #0000315603 (NC_000005.9:g.147494001G>A, NM_001127698.1:c.1964G>A (SPINK5))
Chromosome |
5 |
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.147494001G>A |
DNA change (hg38) |
g.148114438G>A |
Published as |
SPINK5(NM_001127698.1):c.1964G>A (p.G655D, p.(Gly655Asp)), SPINK5(NM_006846.4):c.1964G>A (p.G655D) |
ISCN |
- |
DB-ID |
SPINK5_000031 See all 3 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) |
0.00267 View details |
Owner |
VKGL-NL_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2018-01-15 20:58:59 +01:00 (CET) |
Date last edited |
2023-01-11 15:44:22 +01:00 (CET) |

Variant on transcripts
|