Variant #0000693688 (NC_000023.10:g.64141701T>C, ZC4H2(NM_018684.3):c.221A>G)

Chromosome X
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.64141701T>C
DNA change (hg38) -
Published as ZC4H2(NM_018684.3):c.221A>G (p.N74S)
ISCN -
DB-ID ZC4H2_000035
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) Variant not found in online data sets
Owner VKGL-NL_Groningen
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZC4H2 NM_018684.3 ?/. - c.221A>G r.(?) p.(Asn74Ser)