Variant #0000334612 (NC_000023.10:g.71354553T>C, NM_001013627.2:c.759T>C (NHSL2))

Chromosome X
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.71354553T>C
DNA change (hg38) g.72134703T>C
Published as NHSL2(NM_001013627.2):c.759T>C (p.?)
ISCN -
DB-ID NHSL2_000054
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) 1.0E-5 View details
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 2020-07-20 15:06:38 +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.759T>C r.(?) p.(Ser253=)
RGAG4 NM_001024455.3 ?/. - c.-3163A>G r.(?) p.(=)


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