Variant #0000575107 (NC_000023.10:g.17744556T>C, NHS(NM_198270.2):c.2267T>C)
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.17744556T>C |
DNA change (hg38) |
g.17726436T>C |
Published as |
NHS(NM_001136024.2):c.1799T>C (p.(Phe600Ser)), NHS(NM_001291867.1):c.2330T>C (p.F777S), NHS(NM_001291867.2):c.2330T>C (p.F777S), NHS(NM_198270.4):c... |
ISCN |
- |
DB-ID |
NHS_000067 See all 5 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) |
0.00077 View details |
Owner |
VKGL-NL_Groningen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Groningen |

Variant on transcripts
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