Variant #0000893396 (NC_000017.10:g.2585092G>A, NM_000430.3:c.1229G>A (PAFAH1B1))

Chromosome 17
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.2585092G>A
DNA change (hg38) -
Published as PAFAH1B1(NM_000430.3):c.1229G>A (p.R410H), PAFAH1B1(NM_000430.4):c.1229G>A (p.R410H)
ISCN -
DB-ID PAFAH1B1_000025 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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2022-11-01 13:41:49 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PAFAH1B1 NM_000430.3 ?/. - c.1229G>A r.(?) p.(Arg410His)


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