I have a list of SNPs from dbSNP build 150, I want to run a batch analysis on SIFT which uses an older build of rsid's (build 138 - if I'm not mistaken).
I understand that dbSNP rsids are updated based to avoid synonymous occurrences, but could someone please clarify on how would I map the rsids to an older build which is required by SIFT?
Is there any way of confirming the build for my current list of IDs?
Can different genome assemblies have the same rsIDs?
1 answer
y on how would I map the rsids to an older build which is required by SIFT?
dbsnps is available for several builds:
ftp://ftp.ncbi.nih.gov/snp/organisms/human_9606_b150_GRCh37p13/
ftp://ftp.ncbi.nih.gov/snp/organisms/human_9606_b151_GRCh38p7/
Can different genome assemblies have the same rsIDs?
yes e.g rs25
https://www.ncbi.nlm.nih.gov/projects/SNP/snp_ref.cgi?rs=25
GRCh38.p7 108 7 11544515 NT_007819.18 11534515 Rev T Fwd view mapup
GRCh37.p13 105 7 11584142 NT_007819.17 11574142 Rev T Fwd view blast
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