Genomic variant #0000566282

Chromosome 19
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.13934296A>G
DNA change (hg38) -
Published as ZSWIM4(NM_023072.2):c.1846A>G (p.(Met616Val))
ISCN -
DB-ID ZSWIM4_000002
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (large NGS studies) 0.01953 View details
Owner VKGL-NL




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

ClassClinical     

RNA change     

Protein     
ZSWIM4 NM_023072.2 -?/. - c.1846A>G likely benign r.(?) p.(Met616Val)