Variant #0000297645 (NC_000007.13:g.103138251C>T, NC_000007.13(NM_005045.3):c.8950+16G>A (RELN))

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.103138251C>T
DNA change (hg38) g.103497804C>T
Published as RELN(NM_005045.4):c.8950+16G>A, RELN(NM_173054.2):c.8950+16G>A
ISCN -
DB-ID RELN_000174 See all 3 reported entries
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) 0.00383 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RELN NM_005045.3 -/. - c.8950+16G>A r.(=) p.(=)
SLC26A5 NM_198999.2 -/. - c.-51889G>A r.(?) p.(=)


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