Variant #0000624449 (NC_000023.10:g.138711901T>C, NM_005369.4:c.391A>G (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.138711901T>C
DNA change (hg38) g.139629742T>C
Published as MCF2(NM_001171876.1):c.571A>G (p.I191V)
ISCN -
DB-ID MCF2_000057
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) 1.0E-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 2019-12-06 12:43:26 +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.571A>G r.(?) p.(Ile191Val)
MCF2 NM_005369.4 -?/. - c.391A>G r.(?) p.(Ile131Val)


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