Variant #0000969652 (NC_000019.9:g.2249599del, NM_000479.3:c.268del (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.2249599del
DNA change (hg38) -
Published as AMH(NM_000479.5):c.268delG (p.A90Pfs*49)
ISCN -
DB-ID JSRP1_000020
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2024-02-26 20:06:56 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AMH NM_000479.3 +/. - c.268del r.(?) p.(Ala90Profs*49)
SF3A2 NM_007165.4 +/. - c.*1054del r.(?) p.(=)
JSRP1 NM_144616.3 +/. - c.*2731del r.(?) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.