Variant #0000915182 (NC_000019.9:g.2251285C>T, NM_000479.3:c.1012C>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.2251285C>T
DNA change (hg38) -
Published as AMH(NM_000479.5):c.1012C>T (p.R338C)
ISCN -
DB-ID JSRP1_000017
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) 2.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-01-11 15:44:22 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AMH NM_000479.3 ?/. - c.1012C>T r.(?) p.(Arg338Cys)
SF3A2 NM_007165.4 ?/. - c.*2740C>T r.(=) p.(=)
JSRP1 NM_144616.3 ?/. - c.*1043G>A r.(=) p.(=)


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