Variant #0000518490 (NC_000003.11:g.170723276G>A, SLC2A2(NM_000340.1):c.776-15C>T)
Chromosome |
3 |
Allele |
Unknown |
Affects function (as reported) |
Does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.170723276G>A |
DNA change (hg38) |
g.171005487G>A |
Published as |
- |
ISCN |
- |
DB-ID |
SLC2A2_000012 |
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) |
0.14208 View details |
Owner |
VKGL-NL_Nijmegen |

Variant on transcripts
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