Variant #0000324551 (NC_000016.9:g.4555593A>G, NM_020677.3:c.-31073T>C (NMRAL1))

Chromosome 16
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.4555593A>G
DNA change (hg38) g.4505592A>G
Published as HMOX2(NM_001127204.1):c.68A>G (p.(Glu23Gly))
ISCN -
DB-ID HMOX2_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) 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HMOX2 NM_001127204.1 -?/. - c.68A>G r.(?) p.(Glu23Gly)
NMRAL1 NM_020677.3 -?/. - c.-31073T>C r.(?) p.(=)


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