Variant #0000808801 (NC_000019.9:g.2250659C>A, NM_000479.3:c.564C>A (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.2250659C>A
DNA change (hg38) -
Published as AMH(NM_000479.4):c.564C>A (p.C188*)
ISCN -
DB-ID JSRP1_000014 See all 2 reported entries
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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AMH NM_000479.3 +/. - c.564C>A r.(?) p.(Cys188*)
SF3A2 NM_007165.4 +/. - c.*2114C>A r.(=) p.(=)
JSRP1 NM_144616.3 +/. - c.*1669G>T r.(=) p.(=)
MIR4321 NR_036207.1 +/. - n.22C>A r.(?) -


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