Variant #0000623965 (NC_000019.9:g.2251386G>A, NM_000479.3:c.1113G>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.2251386G>A
DNA change (hg38) g.2251387G>A
Published as AMH(NM_000479.5):c.1113G>A (p.W371*)
ISCN -
DB-ID JSRP1_000010
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 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AMH NM_000479.3 +/. - c.1113G>A r.(?) p.(Trp371Ter)
SF3A2 NM_007165.4 +/. - c.*2841G>A r.(=) p.(=)
JSRP1 NM_144616.3 +/. - c.*942C>T r.(=) p.(=)


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