Variant #0000260842 (NC_000012.11:g.53823187_53823190del, NC_000012.11(NM_020547.2):c.968-50_968-47del (AMHR2))

Chromosome 12
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.53823187_53823190del
DNA change (hg38) g.53429403_53429406del
Published as AMHR2(NM_020547.3):c.968-50_968-47delAAGA
ISCN -
DB-ID AMHR2_000012
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_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     
AMHR2 NM_020547.2 -/. - c.968-50_968-47del r.(=) p.(=)


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