Variant #0000923255 (NC_000001.10:g.91809014C>T, NM_001017975.3:c.2308G>A (HFM1))

Chromosome 1
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.91809014C>T
DNA change (hg38) -
Published as HFM1(NM_001017975.6):c.2308G>A (p.D770N)
ISCN -
DB-ID HFM1_000010
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) 0.00184 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-04-16 21:50:28 +02:00 (CEST)
Date last edited 2024-10-29 20:49:11 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HFM1 NM_001017975.3 ?/. - c.2308G>A r.(?) p.(Asp770Asn)
HFM1 NM_001017975.6 ?/. - c.2308G>A r.(?) p.(Asp770Asn)


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