Variant #0000323752 (NC_000014.8:g.74179992T>G, NM_194278.3:c.*6012A>C (ELMSAN1))

Chromosome 14
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.74179992T>G
DNA change (hg38) g.73713289T>G
Published as PNMA1(NM_006029.4):c.351A>C (p.(Gln117His))
ISCN -
DB-ID PNMA1_000001
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) 0.00176 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PNMA1 NM_006029.4 ?/. - c.351A>C r.(?) p.(Gln117His)
ELMSAN1 NM_194278.3 ?/. - c.*6012A>C r.(=) p.(=)


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