Variant #0000692733 (NC_000019.9:g.2249366T>G, NM_000479.3:c.35T>G (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.2249366T>G
DNA change (hg38) -
Published as AMH(NM_000479.3):c.35T>G (p.(Val12Gly)), AMH(NM_000479.4):c.35T>G (p.V12G)
ISCN -
DB-ID JSRP1_000011 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) 0.0014 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 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AMH NM_000479.3 ?/. - c.35T>G r.(?) p.(Val12Gly)
SF3A2 NM_007165.4 ?/. - c.*821T>G r.(=) p.(=)
JSRP1 NM_144616.3 ?/. - c.*2962A>C r.(=) p.(=)


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