Variant #0000527334 (NC_000006.11:g.138201240A>C, TNFAIP3(NM_006290.3):c.1939A>C)
Chromosome |
6 |
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.138201240A>C |
DNA change (hg38) |
g.137880103A>C |
Published as |
TNFAIP3(NM_001270507.1):c.1939A>C (p.T647P), TNFAIP3(NM_001270508.2):c.1939A>C (p.T647P) |
ISCN |
- |
DB-ID |
TNFAIP3_000014 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) |
0.00188 View details |
Owner |
VKGL-NL_Utrecht |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Utrecht |

Variant on transcripts
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