Variant #0000566566 (NC_000019.9:g.17927754C>T, NM_014256.3:c.*4823C>T (B3GNT3))

Chromosome 19
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.17927754C>T
DNA change (hg38) g.17816945C>T
Published as INSL3(NM_001265587.1):c.400G>A (p.A134T)
ISCN -
DB-ID B3GNT3_000003
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) 0.00071 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
INSL3 NM_005543.3 -?/. - c.305G>A r.(?) p.(Arg102His)
B3GNT3 NM_014256.3 -?/. - c.*4823C>T r.(=) p.(=)


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