Variant #0000808802 (NC_000019.9:g.2251178G>A, NM_000479.3:c.905G>A (AMH))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.2251178G>A
DNA change (hg38) -
Published as AMH(NM_000479.4):c.905G>A (p.R302Q)
ISCN -
DB-ID JSRP1_000015
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) 7.0E-5 View details
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.905G>A r.(?) p.(Arg302Gln)
SF3A2 NM_007165.4 +?/. - c.*2633G>A r.(=) p.(=)
JSRP1 NM_144616.3 +?/. - c.*1150C>T r.(=) p.(=)


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