Variant #0000809967 (NC_000023.10:g.138714580C>T, NM_005369.4:c.85G>A (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.138714580C>T
DNA change (hg38) -
Published as MCF2(NM_001171876.1):c.265G>A (p.V89I)
ISCN -
DB-ID MCF2_000060
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) 4.0E-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 2021-09-17 14:40:49 +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.265G>A r.(?) p.(Val89Ile)
MCF2 NM_005369.4 ?/. - c.85G>A r.(?) p.(Val29Ile)


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