Variant #0000530044 (NC_000007.13:g.100245135G>A, NM_003227.3:c.-6003C>T (TFR2))

Chromosome 7
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.100245135G>A
DNA change (hg38) g.100647512G>A
Published as ACTL6B(NM_016188.4):c.691C>T (p.(Pro231Ser))
ISCN -
DB-ID ACTL6B_000007
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 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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TFR2 NM_003227.3 -?/. - c.-6003C>T r.(?) p.(=)
ACTL6B NM_016188.4 -?/. - c.691C>T r.(?) p.(Pro231Ser)


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