Variant #0000566767 (NC_000019.9:g.2250884_2250885insCA, NM_000479.3:c.701_702insCA (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.2250884_2250885insCA
DNA change (hg38) g.2250885_2250886insCA
Published as AMH(NM_000479.4):c.701_702insCA (p.F235Sfs*12)
ISCN -
DB-ID JSRP1_000006
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-15 09:58:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AMH NM_000479.3 +/. - c.701_702insCA r.(?) p.(Phe235SerfsTer12)
SF3A2 NM_007165.4 +/. - c.*2339_*2340insCA r.(=) p.(=)
JSRP1 NM_144616.3 +/. - c.*1443_*1444insTG r.(=) p.(=)


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