Variant #0000991145 (NC_000001.10:g.31837000A>G, NM_004102.3:c.*1733T>C (FABP3))

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.31837000A>G
DNA change (hg38) -
Published as ZCCHC17(NM_001282567.1):c.692A>G (p.(Lys229Arg))
ISCN -
DB-ID FABP3_000001
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 2024-08-28 13:07:21 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FABP3 NM_004102.3 ?/. - c.*1733T>C r.(=) p.(=)
ZCCHC17 NM_016505.2 ?/. - c.686A>G r.(?) p.(Lys229Arg)


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