Variant #0000081767 (NC_000023.10:g.74291351A>C, NM_004299.4:c.1203T>G (ABCB7))
| Chromosome |
X |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.74291351A>C |
| DNA change (hg38) |
g.75071516A>C |
| Published as |
1200T>G, I400M |
| ISCN |
- |
| DB-ID |
ABCB7_000001 See all 3 reported entries |
| Variant remarks |
cloned in yeast ATM1 (V365M), partial loss of function (reduced growth rate iron limiting conditions) |
| Reference |
PubMed: Allikmets 1999, OMIM:var0001 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
1 |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2009-02-01 12:53:15 +01:00 (CET) |
| Date last edited |
2020-07-20 15:28:32 +02:00 (CEST) |

Variant on transcripts
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