Variant #0000657271 (NC_000013.10:g.31722635_31722637del, NC_000013.10(NM_006644.2):c.1138-6_1138-4del (HSPH1))

Chromosome 13
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.31722635_31722637del
DNA change (hg38) g.31148498_31148500del
Published as HSPH1(NM_006644.3):c.1138-6_1138-4delTTT
ISCN -
DB-ID HSPH1_000008 See all 2 reported entries
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2020-07-03 14:38:17 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HSPH1 NM_006644.2 -/. - c.1138-6_1138-4del r.spl? p.?


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