Variant #0000315894 (NC_000023.10:g.7268072G>C, NM_012080.4:c.-201918C>G (HDHD1))

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.7268072G>C
DNA change (hg38) g.7350031G>C
Published as STS(NM_000351.4):c.1522G>C (p.(Asp508His)), STS(NM_000351.5):c.1522G>C (p.D508H)
ISCN -
DB-ID STS_000042 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) 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HDHD1 NM_012080.4 ?/. - c.-201918C>G r.(?) p.(=)


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