Variant #0000618727 (NC_000023.10:g.102979905G>A, NM_001024452.2:c.123C>T (GLRA4))

Chromosome X
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.102979905G>A
DNA change (hg38) g.103724977G>A
Published as GLRA4(NM_001172285.1):c.123C>T (p.P41=)
ISCN -
DB-ID GLRA4_000020
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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-07-20 18:45:01 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GLRA4 NM_001024452.2 -?/. - c.123C>T r.(?) p.(Pro41=)
TMEM31 NM_182541.2 -?/. - c.*10979G>A r.(=) p.(=)


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