Variant #0000262964 (NC_000003.11:g.97499441T>C, NC_000003.11(NM_001278293.1):c.186-18T>C (ARL6))
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.97499441T>C |
DNA change (hg38) |
g.97780597T>C |
Published as |
ARL6(NM_032146.5):c.186-18T>C |
ISCN |
- |
DB-ID |
ARL6_000031 |
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) |
0.02124 View details |
Owner |
VKGL-NL_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2018-01-15 20:58:59 +01:00 (CET) |
Date last edited |
2019-12-06 12:43:26 +01:00 (CET) |

Variant on transcripts
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