Variant #0000924234 (NC_000005.9:g.130498322C>T, NM_005340.6:c.159G>A (HINT1))

Chromosome 5
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.130498322C>T
DNA change (hg38) -
Published as HINT1(NM_005340.7):c.159G>A (p.L53=)
ISCN -
DB-ID HINT1_000011
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) 0.00013 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2023-04-16 21:50:28 +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     
HINT1 NM_005340.5 -?/. - c.159G>A r.(?) p.(Leu53=)
HINT1 NM_005340.6 -?/. - c.159G>A r.(?) p.(Leu53=)


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