Variant #0000269427 (NC_000006.11:g.31910938G>T, NC_000006.11(NM_000063.4):c.1360+62G>T (C2))

Chromosome 6
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.31910938G>T
DNA change (hg38) g.31943161G>T
Published as C2(NM_000063.4):c.1360+62G>T
ISCN -
DB-ID C2_000004
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
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     
C2 NM_000063.4 -/. - c.1360+62G>T r.(=) p.(=)
CFB NM_001710.5 -/. - c.-3061G>T r.(?) p.(=)
ZBTB12 NM_181842.2 -/. - c.-41345C>A r.(?) p.(=)


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