Variant #0000892050 (NC_000015.9:g.43821328C>T, NM_002373.5:c.7657C>T (MAP1A))

Chromosome 15
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.43821328C>T
DNA change (hg38) -
Published as MAP1A(NM_002373.6):c.7657C>T (p.H2553Y)
ISCN -
DB-ID MAP1A_000014
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) 4.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2022-11-01 13:41:49 +01:00 (CET)
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.7657C>T r.(?) p.(His2553Tyr)
PPIP5K1 NM_014659.5 ?/. - c.*5544G>A r.(=) p.(=)


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