Variant #0000340452 (NC_000011.9:g.76922868C>T, NM_000260.3:c.6240C>T (MYO7A))

Chromosome 11
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.76922868C>T
DNA change (hg38) g.77211823C>T
Published as -
ISCN -
DB-ID MYO7A_000036 See all 19 reported entries
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) 0.02587 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-01 10:52:15 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
MYO7A NM_000260.3 -/. - c.6240C>T r.(?) p.(Ser2080=) -
GDPD4 NM_182833.1 -/. - c.*5454G>A r.(=) p.(=) -


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