Variant #0001002377 (NC_000016.9:g.4797585_4797594del, NM_139170.2:c.1522_1531del (C16orf71))

Chromosome 16
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.4797585_4797594del
DNA change (hg38) -
Published as C16orf71(NM_139170.3):c.1522_1531del (p.(Ala508ArgfsTer3))
ISCN -
DB-ID C16orf71_000002
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 2025-11-01 13:22:20 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZNF500 NM_021646.1 ?/. - c.*4791_*4800del r.(=) p.(=)
C16orf71 NM_139170.2 ?/. - c.1522_1531del r.(?) p.(Ala508Argfs*3)


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