Variant #0000554955 (NC_000015.9:g.59500180C>G, NC_000015.9(NM_004998.3):c.1530+700G>C (MYO1E))

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.59500180C>G
DNA change (hg38) g.59207981C>G
Published as LDHAL6B(NM_033195.2):c.1041C>G (p.(Asn347Lys))
ISCN -
DB-ID LDHAL6B_000002
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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYO1E NM_004998.3 ?/. - c.1530+700G>C r.(=) p.(=)
LDHAL6B NM_033195.2 ?/. - c.1041C>G r.(?) p.(Asn347Lys)


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