Variant #0000322321 (NC_000011.9:g.66055687C>A, NM_153266.3:c.-3798C>A (TMEM151A))

Chromosome 11
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.66055687C>A
DNA change (hg38) g.66288216C>A
Published as YIF1A(NM_020470.2):c.108G>T (p.(Gln36His))
ISCN -
DB-ID YIF1A_000001
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 2018-01-15 20:58:59 +01:00 (CET)
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     
YIF1A NM_020470.2 ?/. - c.108G>T r.(?) p.(Gln36His)
TMEM151A NM_153266.3 ?/. - c.-3798C>A r.(?) p.(=)
CNIH2 NM_182553.2 ?/. - c.*4619C>A r.(=) p.(=)


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