Variant #0001037200 (NC_000009.11:g.131353848G>T, NM_001130438.2:c.3099G>T (SPTAN1))
Chromosome |
9 |
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.131353848G>T |
DNA change (hg38) |
- |
Published as |
SPTAN1(NM_001130438.2):c.3099G>T (p.(Glu1033Asp), p.E1033D), SPTAN1(NM_001130438.3):c.3099G>T (p.E1033D) |
ISCN |
- |
DB-ID |
SPTAN1_000014 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) |
4.0E-5 View details |
Owner |
VKGL-NL_Groningen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Groningen |
Date created |
2025-05-05 21:14:00 +02:00 (CEST) |
Date last edited |
N/A |

Variant on transcripts
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