Variant #0000285134 (NC_000011.9:g.18305355C>T, NM_181507.1:c.3045G>A (HPS5))

Chromosome 11
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.18305355C>T
DNA change (hg38) g.18283808C>T
Published as HPS5(NM_181507.1):c.3045G>A (p.M1015I), HPS5(NM_181507.2):c.3045G>A (p.M1015I)
ISCN -
DB-ID HPS5_000013 See all 2 reported entries
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) 0.00533 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
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     
SAA1 NM_000331.4 -?/. - c.*13953C>T r.(=) p.(=)
HPS5 NM_181507.1 -?/. - c.3045G>A r.(?) p.(Met1015Ile)


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