Variant #0000566766 (NC_000019.9:g.2250484dup, NC_000019.9(NM_000479.3):c.555+6dup (AMH))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.2250484dup
DNA change (hg38) g.2250485dup
Published as AMH(NM_000479.3):c.555+5_555+6insA (p.?), AMH(NM_000479.4):c.555+6dupA
ISCN -
DB-ID AMH_000012 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2019-12-04 15:24:38 +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.555+6dup r.(=) p.(=)
SF3A2 NM_007165.4 -?/. - c.*1939dup r.(?) p.(=)
JSRP1 NM_144616.3 -?/. - c.*1844dup r.(?) p.(=)


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