Variant #0000622162 (NC_000009.11:g.130259561C>T, NM_138361.5:c.1860C>T (LRSAM1))
Chromosome |
9 |
Allele |
Unknown |
Affects function (as reported) |
Probably does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
likely benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.130259561C>T |
DNA change (hg38) |
g.127497282C>T |
Published as |
LRSAM1(NM_138361.5):c.1860C>T (p.H620=) |
ISCN |
- |
DB-ID |
LRSAM1_000037 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) |
0.00049 View details |
Owner |
VKGL-NL_Utrecht |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Utrecht |
Date created |
2019-12-06 12:43:26 +01:00 (CET) |
Date last edited |
2020-06-25 18:20:06 +02:00 (CEST) |

Variant on transcripts
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