Variant #0000560639 (NC_000017.10:g.19290132_19290134dup, NM_139033.2:c.*3588_*3590dup (MAPK7))

Chromosome 17
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.19290132_19290134dup
DNA change (hg38) g.19386819_19386821dup
Published as MFAP4(NM_001198695.1):c.105_107dupGCT (p.L37dup)
ISCN -
DB-ID MAPK7_000002
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MFAP4 NM_002404.2 -/. - c.33_35dup r.(?) p.(Leu13dup)
MAPK7 NM_139033.2 -/. - c.*3588_*3590dup r.(=) p.(=)


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