Variant #0000886843 (NC_000005.9:g.38493836G>T, NM_002310.5:c.1937C>A (LIFR))
| Chromosome |
5 |
| 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.38493836G>T |
| DNA change (hg38) |
- |
| Published as |
LIFR(NM_001127671.1):c.1937C>A (p.(Thr646Asn)), LIFR(NM_001127671.2):c.1937C>A (p.T646N), LIFR(NM_002310.6):c.1937C>A (p.T646N) |
| ISCN |
- |
| DB-ID |
LIFR_000027 See all 3 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) |
0.00201 View details |
| Owner |
VKGL-NL_VUmc |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_VUmc |
| Date created |
2022-11-01 13:01:21 +01:00 (CET) |
| Date last edited |
2024-04-19 20:27:30 +02:00 (CEST) |

Variant on transcripts
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