Variant #0000532701 (NC_000007.13:g.794471A>G, NC_000007.13(NM_017802.3):c.1257+13A>G (HEATR2))

Chromosome 7
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.794471A>G
DNA change (hg38) g.754834A>G
Published as DNAAF5(NM_017802.4):c.1257+13A>G
ISCN -
DB-ID HEATR2_000011
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) 0.82027 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 2019-07-18 18:22:55 +02:00 (CEST)
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     
PRKAR1B NM_001164758.1 -/. - c.-27267T>C r.(?) p.(=)
HEATR2 NM_017802.3 -/. - c.1257+13A>G r.(=) p.(=)


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