Variant #0000554314 (NC_000015.9:g.43821376dup, NM_002373.5:c.7705dup (MAP1A))

Chromosome 15
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.43821376dup
DNA change (hg38) g.43529178dup
Published as MAP1A(NM_002373.5):c.7705dup (p.(Arg2569ProfsTer8))
ISCN -
DB-ID MAP1A_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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-06 13:10:08 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MAP1A NM_002373.5 -?/. - c.7705dup r.(?) p.(Arg2569ProfsTer8)
PPIP5K1 NM_014659.5 -?/. - c.*5500dup r.(?) p.(=)


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