115267193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: 3 prime UTR variant
orthologous variants: 46415687-G-T

115267634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: 3 prime UTR variant
orthologous variants: 46416100-T-C

115267638-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: 3 prime UTR variant
orthologous variants: 46416104-C-G

115267638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: 3 prime UTR variant
orthologous variants: 46416104-C-T

http://identifiers.org/hco/5/GRCh38#115267690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46416147-C-A

115267690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: 3 prime UTR variant
orthologous variants: 46416147-C-T

115267696-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: 3 prime UTR variant
orthologous variants: 46416153-G-C

115267696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: 3 prime UTR variant
orthologous variants: 46416153-G-T

http://identifiers.org/hco/5/GRCh38#115267754-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46416201-A-C

115267754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: 3 prime UTR variant
orthologous variants: 46416201-A-G

115267758-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: 3 prime UTR variant
orthologous variants: 46416205-T-A

115267758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: 3 prime UTR variant
orthologous variants: 46416205-T-C

115267834-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: 3 prime UTR variant
orthologous variants: 46416278-G-T

115267883-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: missense variant
orthologous variants: 46416318-C-G

115267883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: missense variant
orthologous variants: 46416318-C-T

115267921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 46416356-A-G

115267921-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 46416356-A-T

115268031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron variant
orthologous variants: 46416442-G-A

115268031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron variant
orthologous variants: 46416442-G-T

115268040-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron variant
orthologous variants: 46416451-G-C

115268046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron variant
orthologous variants: 46416457-A-G

115268742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron variant
orthologous variants: 46416629-A-G

115268760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron variant
orthologous variants: 46416646-A-G

http://identifiers.org/hco/5/GRCh38#115268761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46416647-C-A

115268835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron variant
orthologous variants: 46416702-G-A

115268835-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron variant
orthologous variants: 46416702-G-C

115268835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron variant
orthologous variants: 46416702-G-T

115268849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron variant
orthologous variants: 46416712-A-G

115268849-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron variant
orthologous variants: 46416712-A-T

115269022-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron variant
orthologous variants: 46416884-T-A

115269022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron variant
orthologous variants: 46416884-T-C

http://identifiers.org/hco/5/GRCh38#115269025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46416887-C-A

115269025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron variant
orthologous variants: 46416887-C-T

http://identifiers.org/hco/5/GRCh38#115269068-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46416923-A-C

115269068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron variant
orthologous variants: 46416923-A-G

115269068-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron variant
orthologous variants: 46416923-A-T

115269075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron variant
orthologous variants: 46416930-G-A

115269075-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron variant
orthologous variants: 46416930-G-C

115269075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron variant
orthologous variants: 46416930-G-T

115269213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron variant
orthologous variants: 46417035-A-G

http://identifiers.org/hco/5/GRCh38#115269250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46417058-C-A

115269250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron variant
orthologous variants: 46417058-C-T

115269318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron variant
orthologous variants: 46417123-G-A

115269379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron variant
orthologous variants: 46417180-A-G

115269697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 46418674-G-A

115269697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 46418674-G-T

115269784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 46418761-A-G

115269784-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 46418761-A-T

115269821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46418808-A-G

115270043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46419011-T-C

115270147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46419127-T-C

115270154-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46419134-T-A

115270154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46419134-T-C

115270154-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46419134-T-G

115270223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46419208-T-C

http://identifiers.org/hco/5/GRCh38#115270856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46419646-C-A

115270856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46419646-C-T

http://identifiers.org/hco/5/GRCh38#115271120-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46420322-A-C

115271120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46420322-A-G

115271177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46420384-G-A

115271177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46420384-G-T

http://identifiers.org/hco/5/GRCh38#115271183-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46420387-A-C

115271183-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46420387-A-T

115271230-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 46420434-A-T

115271264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 46420468-C-T

http://identifiers.org/hco/5/GRCh38#115271426-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46420630-A-C

115271439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 46420643-A-G

115271439-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 46420643-A-T

115271459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 46420663-C-T

115271505-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 46420709-T-G

115271527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 46420731-G-A

115271659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron variant
orthologous variants: 46420861-G-A

115271659-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron variant
orthologous variants: 46420861-G-C

115271659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron variant
orthologous variants: 46420861-G-T

http://identifiers.org/hco/5/GRCh38#115271678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46420886-C-A

http://identifiers.org/hco/5/GRCh38#115271721-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46420924-A-C

115271825-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron variant
orthologous variants: 46421029-C-G

115272732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron variant
orthologous variants: 46421661-G-A

115272755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron variant
orthologous variants: 46421683-T-C

http://identifiers.org/hco/5/GRCh38#115272864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46421808-C-A

115272864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron variant
orthologous variants: 46421808-C-T

http://identifiers.org/hco/5/GRCh38#115272981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46421918-C-A

115273220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron variant
orthologous variants: 46422139-G-A

115273449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron variant
orthologous variants: 46422334-C-T

115273515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron variant
orthologous variants: 46422384-A-G

115273653-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron variant
orthologous variants: 46422480-T-G

115274443-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 46423439-C-G

115274589-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 46423547-A-T

http://identifiers.org/hco/5/GRCh38#115275065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46423688-C-A

115275065-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 46423688-C-G

115275065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 46423688-C-T

http://identifiers.org/hco/5/GRCh38#115275115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46423722-C-A

115275115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, missense_variant
orthologous variants: 46423722-C-T

115275125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, splice_region_variant, synonymous_variant
orthologous variants: 46423732-T-C

115275141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron variant
orthologous variants: 46423748-G-T

http://identifiers.org/hco/5/GRCh38#115275145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46423752-C-A

115275145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron variant
orthologous variants: 46423752-C-T

http://identifiers.org/hco/5/GRCh38#115275175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46423776-C-A

115275203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron variant
orthologous variants: 46423803-T-C

115275405-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 46424008-T-G

115275457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 46424060-G-A

115275457-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 46424060-G-C

115275554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 46424157-T-C

115275626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46424230-G-T

115275628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46424232-T-C

115275681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46424290-A-G

115275681-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46424290-A-T

115275826-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46424440-T-G

115275852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46424466-G-A

http://identifiers.org/hco/5/GRCh38#115275857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46424471-C-A

115275857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46424471-C-T

http://identifiers.org/hco/5/GRCh38#115275963-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46424561-A-C

115275963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46424561-A-G

115275963-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46424561-A-T

http://identifiers.org/hco/5/GRCh38#115276203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46424777-C-A

115276203-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46424777-C-G

115276215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46424789-T-C

115276424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46425991-T-C

115276709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46426264-A-G

115276834-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46426383-T-A

115276887-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46426396-A-T

http://identifiers.org/hco/5/GRCh38#115277111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46426603-C-A

115277111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46426603-C-T

115277117-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46426608-T-A

115277119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46426610-T-C

http://identifiers.org/hco/5/GRCh38#115277130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46426620-C-A

115277133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46426623-A-G

115277160-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46426659-T-A

115277160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46426659-T-C

115277178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46426670-A-G

http://identifiers.org/hco/5/GRCh38#115277270-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46426751-A-C

115277692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46427696-G-A

115278829-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46428653-A-T

115279171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46428931-T-C

http://identifiers.org/hco/5/GRCh38#115279187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46428947-C-A

115279187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46428947-C-T

115279199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46428961-A-G

115279256-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46429013-C-G

115279296-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46429053-G-C

115279326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46429076-C-T

115279336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46429091-G-T

115279407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46429147-G-A

115279475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46429217-C-T

http://identifiers.org/hco/5/GRCh38#115279697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46429386-C-A

115279697-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 46429386-C-G

115279697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 46429386-C-T

http://identifiers.org/hco/5/GRCh38#115279717-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46429406-A-C

http://identifiers.org/hco/5/GRCh38#115279756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#46429445-C-A

115279756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 46429445-C-T

115279821-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46429509-G-C

115279821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46429509-G-T

115279938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46429628-A-G

115280027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46429674-T-C

115280027-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46429674-T-G

115280980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46429929-T-C

115280990-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46429934-T-A

115281027-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46429971-T-A

http://identifiers.org/hco/5/GRCh38#115284067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46430425-C-A

115284067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46430425-C-T

http://identifiers.org/hco/5/GRCh38#115284124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46430479-C-A

115284124-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46430479-C-G

http://identifiers.org/hco/5/GRCh38#115284171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46430526-C-A

115284837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 46432391-A-G

115284936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46432489-A-G

115284937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46432490-G-A

115284998-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46432532-G-C

115284998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46432532-G-T

115285089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46432715-T-C

115285184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46432809-T-C

115285184-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46432809-T-G

115285358-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46432957-A-T

115285838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46433186-A-G

115285847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46433194-A-G

115286049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46433344-G-A

http://identifiers.org/hco/5/GRCh38#115286127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46433424-C-A

115286129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46433426-A-G

115286294-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46433558-T-A

115293791-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46440811-G-C

115293791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46440811-G-T

115294515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46442471-T-C

115294633-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46442584-G-C

http://identifiers.org/hco/5/GRCh38#115295526-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46444137-A-C

http://identifiers.org/hco/5/GRCh38#115295800-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46444394-A-C

115295804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46444398-G-A

115295804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46444398-G-T

http://identifiers.org/hco/5/GRCh38#115295968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46444509-C-A

115295968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46444509-C-T

115296105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 46444618-G-T

115296125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46444629-T-C

115296125-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46444629-T-G

http://identifiers.org/hco/5/GRCh38#115296139-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: -A-C

115296139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

http://identifiers.org/hco/5/GRCh38#115296234-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#46444696-A-C

115296234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 46444696-A-G

115296307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 46444729-G-A

115296307-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 46444729-G-C

115296307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 46444729-G-T

http://identifiers.org/hco/5/GRCh38#115296311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#46444733-C-A

115296311-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 46444733-C-G

115296371-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 46444744-A-T

115296419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 46444753-G-A

115296419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 46444753-G-T

115296441-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 46444775-G-C

115296441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 46444775-G-T

http://identifiers.org/hco/5/GRCh38#115296553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46444887-C-A

115296553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 46444887-C-T

http://identifiers.org/hco/5/GRCh38#115296579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46444914-C-A

115296579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 46444914-C-T

115296659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: 5 prime UTR variant
orthologous variants: 46444981-G-A

115296659-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: 5 prime UTR variant
orthologous variants: 46444981-G-C

115296659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28599
most severe consequence: 5 prime UTR variant
orthologous variants: 46444981-G-T