Variant #0000335703 (NC_000023.10:g.138724628G>A, NM_005369.4:c.50C>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.138724628G>A
DNA change (hg38) g.139642469G>A
Published as MCF2(NM_001171877.2):c.50C>T (p.(Ala17Val))
ISCN -
DB-ID MCF2_000013 See all 2 reported entries
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) 0.00164 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 2025-05-05 21:14:00 +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.231+3099C>T r.(=) p.(=)
MCF2 NM_005369.4 -?/. - c.50C>T r.(?) p.(Ala17Val)


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