Variant #0000551483 (NC_000014.8:g.21161931A>G, NM_001097577.2:c.208A>G (ANG))

Chromosome 14
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.21161931A>G
DNA change (hg38) g.20693772A>G
Published as ANG(NM_001145.4):c.208A>G (p.I70V)
ISCN -
DB-ID ANG_000005 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) 0.00075 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2019-12-04 15:24:38 +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.208A>G r.(?) p.(Ile70Val)
RNASE4 NM_002937.3 -?/. - c.-17-5583A>G r.(=) p.(=)


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