Variant #0000262428 (NC_000019.9:g.2251512T>A, NM_000479.3:c.1239T>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.2251512T>A
DNA change (hg38) g.2251513T>A
Published as AMH(NM_000479.4):c.1239T>A (p.G413=), AMH(NM_000479.5):c.1239T>A (p.G413=)
ISCN -
DB-ID AMH_000015 See all 3 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) 0.85378 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 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AMH NM_000479.3 -/. - c.1239T>A r.(?) p.(Gly413=)
SF3A2 NM_007165.4 -/. - c.*2967T>A r.(=) p.(=)
JSRP1 NM_144616.3 -/. - c.*816A>T r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.