Variant #0000262436 (NC_000019.9:g.2249634G>A, NM_000479.3:c.303G>A (AMH))

Chromosome 19
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.2249634G>A
DNA change (hg38) g.2249635G>A
Published as AMH(NM_000479.4):c.303G>A (p.G101=)
ISCN -
DB-ID AMH_000011
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) 0.05953 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 2020-07-15 09:58:11 +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.303G>A r.(?) p.(Gly101=)
SF3A2 NM_007165.4 -/. - c.*1089G>A r.(=) p.(=)
JSRP1 NM_144616.3 -/. - c.*2694C>T r.(=) p.(=)


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