Variant #0000272183 (NC_000003.11:g.15686647C>T, NM_000060.2:c.1284C>T (BTD))

Chromosome 3
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.15686647C>T
DNA change (hg38) g.15645140C>T
Published as BTD(NM_000060.4):c.1284C>T (p.Y428=)
ISCN -
DB-ID BTD_000139
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) 0.00297 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-12 13:37:52 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BTD NM_000060.2 -/. - c.1284C>T r.(?) p.(Tyr428=)
HACL1 NM_012260.2 -/. - c.-43677G>A r.(?) p.(=)


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