Variant #0000993024 (NC_000002.11:g.74480228G>A, NM_006636.3:c.*38859G>A (MTHFD2))

Chromosome 2
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.74480228G>A
DNA change (hg38) -
Published as SLC4A5(NM_133478.2):c.1141C>T (p.(Arg381Cys))
ISCN -
DB-ID MTHFD2_000009
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) 2.0E-5 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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MTHFD2 NM_006636.3 ?/. - c.*38859G>A r.(=) p.(=)
SLC4A5 NM_021196.3 ?/. - c.1141C>T r.(?) p.(Arg381Cys)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.