Variant #0000334617 (NC_000023.10:g.71360097C>T, NM_001013627.2:c.2699C>T (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.71360097C>T
DNA change (hg38) g.72140247C>T
Published as NHSL2(NM_001013627.2):c.2699C>T (p.(Pro900Leu))
ISCN -
DB-ID NHSL2_000061
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NHSL2 NM_001013627.2 -?/. - c.2699C>T r.(?) p.(Pro900Leu)
RGAG4 NM_001024455.3 -?/. - c.-8707G>A r.(?) p.(=)


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