Variant #0000619862 (NC_000023.10:g.71358473C>T, NM_001013627.2:c.1075C>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.71358473C>T
DNA change (hg38) g.72138623C>T
Published as NHSL2(NM_001013627.2):c.1075C>T (p.R359W)
ISCN -
DB-ID NHSL2_000075
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +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.1075C>T r.(?) p.(Arg359Trp)
RGAG4 NM_001024455.3 -?/. - c.-7083G>A r.(?) p.(=)


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