Variant #0000810646 (NC_000023.10:g.71350417A>G, NC_000023.10(NM_001013627.2):c.281-1512A>G (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.71350417A>G
DNA change (hg38) -
Published as RTL5(NM_001024455.3):c.974T>C (p.I325T)
ISCN -
DB-ID NHSL2_000083
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NHSL2 NM_001013627.2 ?/. - c.281-1512A>G r.(=) p.(=)
RGAG4 NM_001024455.3 ?/. - c.974T>C r.(?) p.(Ile325Thr)


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