Variant #0000572747 (NC_000023.10:g.102968730C>A, NC_000023.10(NM_001024452.2):c.934-133G>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.102968730C>A
DNA change (hg38) g.103713802C>A
Published as TMEM31(NM_182541.2):c.311C>A (p.A104D, p.(Ala104Asp))
ISCN -
DB-ID GLRA4_000017 See all 2 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) 1.0E-5 View details
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 2020-08-06 14:59:34 +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.934-133G>T r.(=) p.(=)
TMEM31 NM_182541.2 -?/. - c.311C>A r.(?) p.(Ala104Asp)


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