Variant #0000805868 (NC_000012.11:g.57627779G>A, NC_000012.11(NM_005412.5):c.1280-7G>A (SHMT2))

Chromosome 12
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.57627779G>A
DNA change (hg38) -
Published as SHMT2(NM_001166357.1):c.1217-7G>A
ISCN -
DB-ID NDUFA4L2_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) 0.00013 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 2021-09-17 14:40:49 +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     
SHMT2 NM_005412.5 -?/. - c.1280-7G>A r.(=) p.(=)
NDUFA4L2 NM_020142.3 -?/. - c.*1567C>T r.(=) p.(=)


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