Variant #0000325289 (NC_000017.10:g.19285370C>G, NM_015681.3:c.-19488G>C (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.19285370C>G
DNA change (hg38) g.19382057C>G
Published as MAPK7(NM_002749.3):c.1754C>G (p.(Ser585Cys))
ISCN -
DB-ID MAPK7_000001
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) 0.00033 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MFAP4 NM_002404.2 ?/. - c.*2405G>C r.(=) p.(=)
EPN2 NM_014964.4 ?/. - c.*47803C>G r.(=) p.(=)
B9D1 NM_015681.3 ?/. - c.-19488G>C r.(?) p.(=)
MAPK7 NM_139033.2 ?/. - c.1754C>G r.(?) p.(Ser585Cys)


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