Variant #0000728488 (NC_000023.10:g.138698512G>A, NM_005369.4:c.1120C>T (MCF2))

Chromosome X
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.138698512G>A
DNA change (hg38) -
Published as MCF2(NM_001171876.1):c.1300C>T (p.L434=)
ISCN -
DB-ID MCF2_000059
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) 2.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +01:00 (CET)
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.1300C>T r.(?) p.(Leu434=)
MCF2 NM_005369.4 -?/. - c.1120C>T r.(?) p.(Leu374=)


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