Variant #0000292102 (NC_000014.8:g.64916198G>A, NM_005956.3:c.2315G>A (MTHFD1))

Chromosome 14
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.64916198G>A
DNA change (hg38) g.64449480G>A
Published as MTHFD1(NM_005956.4):c.2315G>A (p.R772H)
ISCN -
DB-ID MTHFD1_000007
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) 0.00179 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 2018-01-15 20:58:59 +01:00 (CET)
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     
ZBTB1 NM_001123329.1 -/. - c.-55485G>A r.(?) p.(=)
AKAP5 NM_004857.3 -/. - c.-16397G>A r.(?) p.(=)
MTHFD1 NM_005956.3 -/. - c.2315G>A r.(?) p.(Arg772His)
ZBTB25 NM_006977.2 -/. - c.*37443C>T r.(=) p.(=)


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