Variant #0000281273 (NC_000014.8:g.31570520G>A, NM_014574.3:c.-75129C>T (STRN3))

Chromosome 14
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.31570520G>A
DNA change (hg38) g.31101314G>A
Published as HECTD1(NM_015382.4):c.7561C>T (p.L2521=)
ISCN -
DB-ID HECTD1_000001
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) 0.00027 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AP4S1 NM_001128126.2 -?/. - c.*8279G>A r.(=) p.(=)
STRN3 NM_014574.3 -?/. - c.-75129C>T r.(?) p.(=)
HECTD1 NM_015382.2 -?/. - c.7561C>T r.(?) p.(Leu2521=)


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