Variant #0000518384 (NC_000003.11:g.158363463A>G, NM_024996.5:c.127A>G (GFM1))

Chromosome 3
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.158363463A>G
DNA change (hg38) g.158645674A>G
Published as GFM1(NM_024996.5):c.127A>G (p.(Asn43Asp))
ISCN -
DB-ID GFM1_000022 See all 3 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) 0.00965 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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LXN NM_020169.3 -?/. - c.*20972T>C r.(=) p.(=)
GFM1 NM_024996.5 -?/. - c.127A>G r.(?) p.(Asn43Asp)


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