Variant #0000806695 (NC_000015.9:g.43821387T>A, NM_002373.5:c.7716T>A (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.43821387T>A
DNA change (hg38) -
Published as MAP1A(NM_002373.6):c.7716T>A (p.P2572=)
ISCN -
DB-ID MAP1A_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) 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 2021-09-17 14:40:49 +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     
MAP1A NM_002373.5 -?/. - c.7716T>A r.(?) p.(Pro2572=)
PPIP5K1 NM_014659.5 -?/. - c.*5485A>T r.(=) p.(=)


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