Variant #0000252530 (NC_000014.8:g.21161845A>T, NM_001097577.2:c.122A>T (ANG))

Chromosome 14
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.21161845A>T
DNA change (hg38) g.20693686A>T
Published as ANG(NM_001145.4):c.122A>T (p.K41I)
ISCN -
DB-ID ANG_000002 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) 0.00117 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 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     
ANG NM_001097577.2 +/. - c.122A>T r.(?) p.(Lys41Ile)
RNASE4 NM_002937.3 +/. - c.-17-5669A>T r.(=) p.(=)


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