Variant #0000262434 (NC_000019.9:g.2249539dup, NM_000479.3:c.208dup (AMH))

Chromosome 19
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.2249539dup
DNA change (hg38) g.2249540dup
Published as AMH(NM_000479.4):c.208dupC (p.L70Pfs*11)
ISCN -
DB-ID AMH_000009
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-15 09:57:46 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AMH NM_000479.3 +/. - c.208dup r.(?) p.(Leu70ProfsTer11)
SF3A2 NM_007165.4 +/. - c.*994dup r.(?) p.(=)
JSRP1 NM_144616.3 +/. - c.*2794dup r.(?) p.(=)


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