Variant #0001054378 (NC_000012.11:g.57626627G>C, NC_000012.11(NM_005412.5):c.857+1G>C (SHMT2))

Chromosome 12
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.57626627G>C
DNA change (hg38) -
Published as SHMT2(NM_005412.6):c.857+1G>C
ISCN -
DB-ID NDUFA4L2_000010
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SHMT2 NM_005412.5 ?/. - c.857+1G>C r.spl? p.?
NDUFA4L2 NM_020142.3 ?/. - c.*2719C>G r.(=) p.(=)


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