Variant #0000530170 (NC_000007.13:g.103151398G>A, NM_005045.3:c.8174C>T (RELN))

Chromosome 7
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.103151398G>A
DNA change (hg38) g.103510951G>A
Published as RELN(NM_005045.4):c.8174C>T (p.S2725F), RELN(NM_173054.2):c.8174C>T (p.S2725F)
ISCN -
DB-ID RELN_000197 See all 2 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) 6.0E-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 2019-07-18 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     
RELN NM_005045.3 ?/. - c.8174C>T r.(?) p.(Ser2725Phe)
SLC26A5 NM_198999.2 ?/. - c.-65036C>T r.(?) p.(=)


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