Variant #0000610271 (NC_000006.11:g.31869065T>A, NM_000063.4:c.-26465T>A (C2))

Chromosome 6
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.31869065T>A
DNA change (hg38) g.31901288T>A
Published as C2(NM_001282457.2):c.-64+3346T>A
ISCN -
DB-ID C2_000027
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) 2.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C2 NM_000063.4 -?/. - c.-26465T>A r.(?) p.(=)
EHMT2 NM_006709.3 -?/. - c.-3611A>T r.(?) p.(=)
ZBTB12 NM_181842.2 -?/. - c.18A>T r.(?) p.(Glu6Asp)


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