Variant #0000307050 (NC_000023.10:g.71349791G>A, NC_000023.10(NM_001013627.2):c.281-2138G>A (NHSL2))

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.71349791G>A
DNA change (hg38) g.72129941G>A
Published as RGAG4(NM_001024455.3):c.1600C>T (p.R534C, p.(Arg534Cys))
ISCN -
DB-ID NHSL2_000045 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) 0.0004 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2019-12-04 15:24:38 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NHSL2 NM_001013627.2 -?/. - c.281-2138G>A r.(=) p.(=)
RGAG4 NM_001024455.3 -?/. - c.1600C>T r.(?) p.(Arg534Cys)


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