Variant #0000993393 (NC_000003.11:g.15672987T>C, NC_000003.11(NM_000060.2):c.45-3944T>C (BTD))

Chromosome 3
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.15672987T>C
DNA change (hg38) -
Published as BTD(NM_001281724.1):c.35T>C (p.(Met12Thr))
ISCN -
DB-ID BTD_000167
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_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.45-3944T>C r.(=) p.(=)
BTD NM_001370658.1 -?/. - c.-16-3944T>C r.(=) p.(=)
HACL1 NM_012260.2 -?/. - c.-30017A>G r.(?) p.(=)


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