Variant #0000993397 (NC_000003.11:g.15685955G>A, NM_000060.2:c.592G>A (BTD))

Chromosome 3
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.15685955G>A
DNA change (hg38) -
Published as BTD(NM_000060.2):c.592G>A (p.(Val198Ile))
ISCN -
DB-ID BTD_000168
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) 2.0E-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 13:16:32 +02:00 (CEST)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BTD NM_000060.2 ?/. - c.592G>A r.(?) p.(Val198Ile)
BTD NM_001370658.1 ?/. - c.532G>A r.(?) p.(Val178Ile)
HACL1 NM_012260.2 ?/. - c.-42985C>T r.(?) p.(=)


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