Variant #0000262433 (NC_000019.9:g.2251930G>T, NM_000479.3:c.1657G>T (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.2251930G>T
DNA change (hg38) g.2251931G>T
Published as AMH(NM_000479.4):c.1657G>T (p.V553L)
ISCN -
DB-ID AMH_000019
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) 0.00032 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +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.1657G>T r.(?) p.(Val553Leu)
SF3A2 NM_007165.4 ?/. - c.*3385G>T r.(=) p.(=)
JSRP1 NM_144616.3 ?/. - c.*398C>A r.(=) p.(=)


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