Variant #0000576955 (NC_000023.10:g.64737944G>T, NM_031206.4:c.1850C>A (LAS1L))
Chromosome |
X |
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.64737944G>T |
DNA change (hg38) |
g.65518064G>T |
Published as |
LAS1L(NM_001170649.1):c.1799C>A (p.(Ser600Tyr)), LAS1L(NM_031206.4):c.1850C>A (p.S617Y), LAS1L(NM_031206.7):c.1850C>A (p.S617Y) |
ISCN |
- |
DB-ID |
LAS1L_000010 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) |
2.0E-5 View details |
Owner |
VKGL-NL_Leiden |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Leiden |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2025-02-07 18:57:27 +01:00 (CET) |

Variant on transcripts
|