Variant #0000969653 (NC_000019.9:g.2249614C>T, NM_000479.3:c.283C>T (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.2249614C>T
DNA change (hg38) -
Published as AMH(NM_000479.5):c.283C>T (p.R95*)
ISCN -
DB-ID JSRP1_000021
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.283C>T r.(?) p.(Arg95*)
SF3A2 NM_007165.4 +/. - c.*1069C>T r.(=) p.(=)
JSRP1 NM_144616.3 +/. - c.*2714G>A r.(=) p.(=)


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