Variant #0000323673 (NC_000014.8:g.50251694C>T, NM_004713.3:c.3102G>A (NEMF))

Chromosome 14
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.50251694C>T
DNA change (hg38) g.49784976C>T
Published as NEMF(NM_004713.3):c.3102G>A (p.(Met1034Ile))
ISCN -
DB-ID NEMF_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) 0.00026 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NEMF NM_004713.3 ?/. - c.3102G>A r.(?) p.(Met1034Ile)
KLHDC2 NM_014315.2 ?/. - c.*2023C>T r.(=) p.(=)


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