Variant #0000924375 (NC_000005.9:g.71495621C>T, NM_005909.3:c.6439C>T (MAP1B))

Chromosome 5
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.71495621C>T
DNA change (hg38) -
Published as MAP1B(NM_005909.5):c.6439C>T (p.P2147S)
ISCN -
DB-ID MAP1B_000018
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-04-16 21:50:28 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MAP1B NM_005909.3 ?/. - c.6439C>T r.(?) p.(Pro2147Ser)


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