Variant #0001003031 (NC_000017.10:g.19282394A>C, NM_015681.3:c.-16512T>G (B9D1))

Chromosome 17
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.19282394A>C
DNA change (hg38) -
Published as MAPK7(NM_002749.3):c.181A>C (p.(Ile61Leu))
ISCN -
DB-ID EPN2_000013
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) 3.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MFAP4 NM_002404.2 ?/. - c.*5381T>G r.(=) p.(=)
EPN2 NM_014964.4 ?/. - c.*44827A>C r.(=) p.(=)
B9D1 NM_015681.3 ?/. - c.-16512T>G r.(?) p.(=)
MAPK7 NM_139033.2 ?/. - c.181A>C r.(?) p.(Ile61Leu)


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