Variant #0000993018 (NC_000002.11:g.74459684T>C, NM_006636.3:c.*18315T>C (MTHFD2))

Chromosome 2
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.74459684T>C
DNA change (hg38) -
Published as SLC4A5(NM_133478.2):c.2686A>G (p.(Thr896Ala))
ISCN -
DB-ID MTHFD2_000003
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 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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MTHFD2 NM_006636.3 -?/. - c.*18315T>C r.(=) p.(=)
SLC4A5 NM_021196.3 -?/. - c.2686A>G r.(?) p.(Thr896Ala)


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