Variant #0000162949 (NC_000008.10:g.22021060G>A, NC_000008.10(NM_003018.3):c.435+1G>A (SFTPC))
| Chromosome |
8 |
| 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.22021060G>A |
| DNA change (hg38) |
g.22163547G>A |
| Published as |
- |
| ISCN |
- |
| DB-ID |
SFTPC_000007 See all 2 reported entries |
| Variant remarks |
consequences on splicing determined using a mini-gene construct |
| Reference |
Fanen, submitted |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Pascale Fanen |
| Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
| Created by |
Pascale Fanen |
| Date created |
2017-02-07 17:43:55 +01:00 (CET) |
| Date last edited |
2020-07-14 21:50:58 +02:00 (CEST) |

Variant on transcripts
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