Variant #0000863618 (NC_000014.8:g.64921543G>A, NM_005956.3:c.2668G>A (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.64921543G>A
DNA change (hg38) -
Published as MTHFD1(NM_005956.4):c.2668G>A (p.D890N)
ISCN -
DB-ID AKAP5_000005
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) 3.0E-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 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZBTB1 NM_001123329.1 ?/. - c.-50140G>A r.(?) p.(=)
AKAP5 NM_004857.3 ?/. - c.-11052G>A r.(?) p.(=)
MTHFD1 NM_005956.3 ?/. - c.2668G>A r.(?) p.(Asp890Asn)
ZBTB25 NM_006977.2 ?/. - c.*32098C>T r.(=) p.(=)


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