Variant #0000925225 (NC_000010.10:g.93394G>A, NM_177987.2:c.938C>T (TUBB8))

Chromosome 10
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.93394G>A
DNA change (hg38) -
Published as TUBB8(NM_177987.2):c.938C>T (p.A313V), TUBB8(NM_177987.3):c.938C>T (p.A313V)
ISCN -
DB-ID TUBB8_000028 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) 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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TUBB8 NM_177987.2 -?/. - c.938C>T r.(?) p.(Ala313Val)


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