Variant #0000260856 (NC_000014.8:g.21162091G>C, NM_001097577.2:c.368G>C (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.21162091G>C
DNA change (hg38) g.20693932G>C
Published as ANG(NM_001145.4):c.368G>C (p.G123A)
ISCN -
DB-ID ANG_000004
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) 0.0001 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.368G>C r.(?) p.(Gly123Ala)
RNASE4 NM_002937.3 -?/. - c.-17-5423G>C r.(=) p.(=)


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