Variant #0000304118 (NC_000023.10:g.17653697C>T, NHS(NM_198270.2):c.566-52165C>T)

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.17653697C>T
DNA change (hg38) g.17635577C>T
Published as NHS(NM_001136024.2):c.11C>T (p.(Ala4Val)), NHS(NM_001136024.3):c.11C>T (p.A4V)
ISCN -
DB-ID NHS_000025 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) 0.00446 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NHS NM_198270.2 -?/. - c.566-52165C>T r.(=) p.(=)