Variant #0000984481 (NC_000023.10:g.138669949T>G, NC_000023.10(NM_005369.4):c.2450-2A>C (MCF2))

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.138669949T>G
DNA change (hg38) -
Published as MCF2(NM_001171876.2):c.2678-2A>C
ISCN -
DB-ID MCF2_000062
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 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MCF2 NM_001171876.1 ?/. - c.2678-2A>C r.spl? p.?
MCF2 NM_005369.4 ?/. - c.2450-2A>C r.spl? p.?


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