Variant #0000619100 (NC_000023.10:g.148044334G>A, NM_002025.3:c.2780G>A (AFF2))
Chromosome |
X |
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.148044334G>A |
DNA change (hg38) |
g.148962804G>A |
Published as |
AFF2(NM_001169122.1):c.2681G>A (p.(Arg894His)), AFF2(NM_002025.3):c.2780G>A (p.R927H), AFF2(NM_002025.4):c.2780G>A (p.R927H) |
ISCN |
- |
DB-ID |
AFF2_000080 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) |
0.00165 View details |
Owner |
VKGL-NL_Utrecht |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Utrecht |
Date created |
2019-12-04 15:24:38 +01:00 (CET) |
Date last edited |
2021-09-17 14:40:49 +02:00 (CEST) |

Variant on transcripts
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