Variant #0000679565 (NC_000012.11:g.50355911G>A, NM_000486.5:c.*6520G>A (AQP2))

Chromosome 12
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.50355911G>A
DNA change (hg38) -
Published as AQP5(NM_001651.3):c.111G>A (p.S37=)
ISCN -
DB-ID AQP2_000019
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AQP2 NM_000486.5 -?/. - c.*6520G>A r.(=) p.(=)
AQP5 NM_001651.2 -?/. - c.111G>A r.(?) p.(Ser37=)
AQP6 NM_001652.3 -?/. - c.-11046G>A r.(?) p.(=)


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