Variant #0000267813 (NC_000018.9:g.33713287T>A, NC_000018.9(NM_018255.2):c.217+8T>A (ELP2))

Chromosome 18
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.33713287T>A
DNA change (hg38) g.36133324T>A
Published as ELP2(NM_001242875.3):c.217+8T>A
ISCN -
DB-ID ELP2_000002
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) 0.34468 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC39A6 NM_001099406.1 -/. - c.-4247A>T r.(?) p.(=)
ELP2 NM_018255.2 -/. - c.217+8T>A r.(=) p.(=)


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