Variant #0001004572 (NC_000019.9:g.2253777G>A, NM_000479.3:c.*1821G>A (AMH))

Chromosome 19
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.2253777G>A
DNA change (hg38) -
Published as JSRP1(NM_144616.3):c.278C>T (p.(Pro93Leu))
ISCN -
DB-ID JSRP1_000022
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) 4.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +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.*1821G>A r.(=) p.(=)
JSRP1 NM_144616.3 ?/. - c.278C>T r.(?) p.(Pro93Leu)


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