Variant #0000552827 (NC_000014.8:g.64921502A>G, NM_005956.3:c.2627A>G (MTHFD1))

Chromosome 14
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.64921502A>G
DNA change (hg38) g.64454784A>G
Published as MTHFD1(NM_005956.4):c.2627A>G (p.E876G)
ISCN -
DB-ID AKAP5_000002
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 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     
ZBTB1 NM_001123329.1 ?/. - c.-50181A>G r.(?) p.(=)
AKAP5 NM_004857.3 ?/. - c.-11093A>G r.(?) p.(=)
MTHFD1 NM_005956.3 ?/. - c.2627A>G r.(?) p.(Glu876Gly)
ZBTB25 NM_006977.2 ?/. - c.*32139T>C r.(=) p.(=)


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