Variant #0000622258 (NC_000009.11:g.34637689C>T, NM_005866.2:c.6G>A (SIGMAR1))
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.34637689C>T |
DNA change (hg38) |
g.34637692C>T |
Published as |
SIGMAR1(NM_001282208.2):c.6G>A (p.Q2=), SIGMAR1(NM_005866.3):c.6G>A (p.Q2=), SIGMAR1(NM_005866.4):c.6G>A (p.Q2=) |
ISCN |
- |
DB-ID |
SIGMAR1_000009 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) |
0.00144 View details |
Owner |
VKGL-NL_AMC |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_AMC |
Date created |
2019-12-06 12:43:26 +01:00 (CET) |
Date last edited |
2023-01-11 15:44:22 +01:00 (CET) |

Variant on transcripts
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