Variant #0000575036 (NC_000023.10:g.154290176C>G, NM_023934.3:c.*7229C>G (FUNDC2))

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.154290176C>G
DNA change (hg38) g.155061901C>G
Published as CMC4(NM_001018024.2):c.149G>C (p.(Cys50Ser)), CMC4(NM_001018024.3):c.149G>C (p.C50S)
ISCN -
DB-ID CMC4_000005 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) 0.00038 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CMC4 NM_001018024.2 -?/. - c.149G>C r.(?) p.(Cys50Ser)
MTCP1 NM_001018025.3 -?/. - c.*3503G>C r.(=) p.(=)
FUNDC2 NM_023934.3 -?/. - c.*7229C>G r.(=) p.(=)


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