Variant #0000888227 (NC_000008.10:g.145638215G>A, NM_013291.2:c.-3557C>T (CPSF1))
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.145638215G>A |
DNA change (hg38) |
- |
Published as |
SLC39A4(NM_017767.2):c.1668C>T (p.V556=), SLC39A4(NM_130849.4):c.1743C>T (p.V581=) |
ISCN |
- |
DB-ID |
CPSF1_000009 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) |
0.00073 View details |
Owner |
VKGL-NL_Utrecht |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Utrecht |
Date created |
2022-11-01 13:01:21 +01:00 (CET) |
Date last edited |
N/A |

Variant on transcripts
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