Variant #0001050044 (NC_000001.10:g.35452796dup, NM_007167.3:c.3893dup (ZMYM6))

Chromosome 1
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.35452796dup
DNA change (hg38) -
Published as ZMYM6(NM_007167.4):c.3893dup (p.(Asn1298Lysfs*48))
ISCN -
DB-ID ZMYM6_000032
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 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZMYM6NB NM_001195156.1 ?/. - c.-1884dup r.(?) p.(=)
ZMYM6 NM_007167.3 ?/. - c.3893dup r.(?) p.(Asn1298Lysfs*48)


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