Variant #0000719079 (NC_000002.11:g.85893771_85893772insTT, NM_198843.2:c.397_398insAA (SFTPB))
| Chromosome |
2 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.85893771_85893772insTT |
| DNA change (hg38) |
- |
| Published as |
SFTPB(NM_198843.2):c.397_398insAA (p.P133Qfs*95), SFTPB(NM_198843.3):c.361_362insAA (p.P121Qfs*95) |
| ISCN |
- |
| DB-ID |
SFTPB_000009 See all 2 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) |
0.00023 View details |
| Owner |
VKGL-NL_Groningen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Groningen |
| Date created |
2021-02-08 18:36:18 +01:00 (CET) |
| Date last edited |
2023-07-07 10:10:56 +02:00 (CEST) |

Variant on transcripts
|