58459351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 3 prime UTR variant
orthologous variants: 173633893-G-A

http://identifiers.org/hco/20/GRCh38#58459579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173634119-C-A

58459579-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 3 prime UTR variant
orthologous variants: 173634119-C-G

58459579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 3 prime UTR variant
orthologous variants: 173634119-C-T

58459630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 3 prime UTR variant
orthologous variants: 173634173-G-A

58459630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 3 prime UTR variant
orthologous variants: 173634173-G-T

58459698-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 3 prime UTR variant
orthologous variants: 173634221-A-T

58459712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 3 prime UTR variant
orthologous variants: 173634235-T-C

58459721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 3 prime UTR variant
orthologous variants: 173634244-G-A

58459799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 3 prime UTR variant
orthologous variants: 173634336-T-C

58459959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 3 prime UTR variant
orthologous variants: 173634478-T-C

58460054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 3 prime UTR variant
orthologous variants: 173634574-T-C

http://identifiers.org/hco/20/GRCh38#58460079-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173634594-A-C

58460079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 3 prime UTR variant
orthologous variants: 173634594-A-G

http://identifiers.org/hco/20/GRCh38#58460241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173634759-C-A

58460241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 3 prime UTR variant
orthologous variants: 173634759-C-T

58460538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 3 prime UTR variant
orthologous variants: 173634992-G-A

58460538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 3 prime UTR variant
orthologous variants: 173634992-G-T

58460598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 3 prime UTR variant
orthologous variants: 173635023-T-C

58460598-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 3 prime UTR variant
orthologous variants: 173635023-T-G

http://identifiers.org/hco/20/GRCh38#58460717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173635124-C-A

58460717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 3 prime UTR variant
orthologous variants: 173635124-C-T

58460718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 3 prime UTR variant
orthologous variants: 173635125-T-C

http://identifiers.org/hco/20/GRCh38#58460738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173635144-C-A

58460738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 3 prime UTR variant
orthologous variants: 173635144-C-T

58460756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 3 prime UTR variant
orthologous variants: 173635164-G-A

58460773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 3 prime UTR variant
orthologous variants: 173635180-T-C

58460859-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: synonymous variant
orthologous variants: 173635267-C-G

58460859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: synonymous variant
orthologous variants: 173635267-C-T

58460887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: missense variant
orthologous variants: 173635301-G-A

58461073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: missense variant
orthologous variants: 173635483-T-C

58461105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: synonymous variant
orthologous variants: 173635515-G-A

58461105-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: missense variant
orthologous variants: 173635515-G-C

58461105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: missense variant
orthologous variants: 173635515-G-T

58461177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 173635587-G-A

http://identifiers.org/hco/20/GRCh38#58461226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173635636-C-A

58461226-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 173635636-C-G

58461226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 173635636-C-T

http://identifiers.org/hco/20/GRCh38#58461370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173635780-C-A

58461370-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 173635780-C-G

58461370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 173635780-C-T

58461375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 173635785-G-A

58461384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 173635794-G-A

58461401-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 173635810-T-G

58461415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 173635824-G-A

58461438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 173635847-G-A

58461438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 173635847-G-T

http://identifiers.org/hco/20/GRCh38#58461455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173635864-C-A

58461455-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 173635864-C-G

58461455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 173635864-C-T

58461465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 173635874-G-A

58461465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 173635874-G-T

http://identifiers.org/hco/20/GRCh38#58461509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173635932-C-A

58461509-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 173635932-C-G

58461509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 173635932-C-T

http://identifiers.org/hco/20/GRCh38#58461543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173635966-C-A

58461543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 173635966-C-T

http://identifiers.org/hco/20/GRCh38#58461560-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173635983-A-C

58461560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 173635983-A-G

58461616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173636031-G-A

58461616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173636031-G-T

58461667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173636077-T-C

58461667-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173636077-T-G

58463531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron variant
orthologous variants: 173637190-C-T

58463756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron variant
orthologous variants: 173637392-G-T

58463830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron variant
orthologous variants: 173637457-C-T

http://identifiers.org/hco/20/GRCh38#58465256-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173638771-A-C

58465352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron variant
orthologous variants: 173638857-G-A

58465440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron variant
orthologous variants: 173638941-C-T

58465863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron variant
orthologous variants: 173639371-A-G

http://identifiers.org/hco/20/GRCh38#58466609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173640672-C-A

http://identifiers.org/hco/20/GRCh38#58466646-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173640709-A-C

58466836-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron variant
orthologous variants: 173640861-C-G

58466836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron variant
orthologous variants: 173640861-C-T

http://identifiers.org/hco/20/GRCh38#58466956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173641010-C-A

58466956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron variant
orthologous variants: 173641010-C-T

58467078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron variant
orthologous variants: 173641105-T-C

http://identifiers.org/hco/20/GRCh38#58467143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173641153-C-A

58467143-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: missense variant
orthologous variants: 173641153-C-G

58467143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: missense variant
orthologous variants: 173641153-C-T

http://identifiers.org/hco/20/GRCh38#58467168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173641178-C-A

58467168-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: missense variant
orthologous variants: 173641178-C-G

58467168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: missense variant
orthologous variants: 173641178-C-T

http://identifiers.org/hco/20/GRCh38#58467218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173641228-C-A

58467218-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: missense variant
orthologous variants: 173641228-C-G

58467218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: missense variant
orthologous variants: 173641228-C-T

http://identifiers.org/hco/20/GRCh38#58467223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173641233-C-A

58467237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: missense variant
orthologous variants: 173641247-G-A

58467237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: missense variant
orthologous variants: 173641247-G-T

http://identifiers.org/hco/20/GRCh38#58467239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173641249-C-A

58467239-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: missense variant
orthologous variants: 173641249-C-G

58467239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: missense variant
orthologous variants: 173641249-C-T

http://identifiers.org/hco/20/GRCh38#58467253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173641263-C-A

58467253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: synonymous variant
orthologous variants: 173641263-C-T

http://identifiers.org/hco/20/GRCh38#58467350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173641360-C-A

58467350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: missense variant
orthologous variants: 173641360-C-T

58467352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: synonymous variant
orthologous variants: 173641362-G-A

58467352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: synonymous variant
orthologous variants: 173641362-G-T

58467362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: missense variant
orthologous variants: 173641372-A-G

58469012-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron variant
orthologous variants: 173642684-A-T

58469580-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron variant
orthologous variants: 173643250-C-G

58469610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron variant
orthologous variants: 173643268-C-T

58469672-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron variant
orthologous variants: 173643320-C-G

58469691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron variant
orthologous variants: 173643337-G-A

58469715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron variant
orthologous variants: 173643365-T-C

58470253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173643810-G-A

58470397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173643978-A-G

58470500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173644088-T-C

58470500-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173644088-T-G

58470512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173644100-A-G

http://identifiers.org/hco/20/GRCh38#58470633-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173644226-A-C

58470633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 173644226-A-G

58470633-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 173644226-A-T

58470685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 173644278-G-A

58470685-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 173644278-G-C

58470685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 173644278-G-T

58470714-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 173644307-C-G

58470714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 173644307-C-T

http://identifiers.org/hco/20/GRCh38#58471227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173644447-C-A

58471227-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173644447-C-G

58471349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173644558-G-A

58471425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173644609-C-T

58471478-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 173644657-C-G

http://identifiers.org/hco/20/GRCh38#58471507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#173644680-C-A

58471507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 173644680-C-T

58471567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173644720-G-A

58471601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 173644734-A-G

58472285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173645334-A-G

58476639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173649026-C-T

http://identifiers.org/hco/20/GRCh38#58476646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173649033-C-A

58476763-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173649143-A-T

58476775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173649151-A-G

58476838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173649198-C-T

58476859-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173649208-T-G

58477209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173649489-T-C

58478058-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173650036-T-A

58478400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173650407-C-T

http://identifiers.org/hco/20/GRCh38#58478471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173650649-C-A

58478471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173650649-C-T

58478781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173650892-G-A

58478910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173650972-G-T

58479189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173651134-T-C

58479291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173651223-A-G

58479292-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173651224-G-C

58479415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173651342-A-G

58479796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173652062-G-A

58479796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173652062-G-T

58479874-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173652122-T-G

58479954-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173652194-G-C

http://identifiers.org/hco/20/GRCh38#58480182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173652403-C-A

http://identifiers.org/hco/20/GRCh38#58480307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173652523-C-A

58480307-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173652523-C-G

58480307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173652523-C-T

58480517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173652716-G-A

58480967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173653153-G-A

58481129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173653275-G-A

58481802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173653946-G-A

58482118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173654238-C-T

58483802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173655903-G-A

58483802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173655903-G-T

58484425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173656423-G-A

58484434-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173656430-G-C

58484617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173656612-T-C

58484617-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173656612-T-G

58484626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173656621-T-C

58484626-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173656621-T-G

58484630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173656625-G-A

58484666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173656657-C-T

58484759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173656750-G-A

58485543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173657735-T-C

58485831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173658049-T-C

58485855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173658073-G-T

58486189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173658375-T-C

58494961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173669207-C-T

58494990-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173669239-C-G

58495016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173669265-C-T

58495354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173669528-A-G

58495376-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173669549-G-C

58495390-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173669563-G-C

58495487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173669632-C-T

58495545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173669682-G-A

58495577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173669717-G-A

58495658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173669776-G-A

58495769-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173669852-T-A

58495770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173669853-A-G

58495873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173669980-G-T

58495883-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173669990-C-G

58495894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173670022-C-T

58495937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173670065-C-T

58496029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173670140-C-T

http://identifiers.org/hco/20/GRCh38#58496210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173670319-C-A

58496300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173670409-C-T

58496356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173670465-G-A

58496359-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173670468-C-G

58497236-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173673594-C-G

58497937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173674470-T-C

58498163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173674697-A-G

58498263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173674797-G-A

58498263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173674797-G-T

58498541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173675071-T-C

58498565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173675095-T-C

http://identifiers.org/hco/20/GRCh38#58498903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173675395-C-A

58498907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173675399-C-T

58498949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173675442-C-T

58498992-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173675485-A-T

58498997-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173675490-G-C

58499127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173675574-T-C

58499230-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173675663-G-C

58499264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173675699-T-C

58503306-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173682296-G-C

58503306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173682296-G-T

58503407-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173682397-A-T

58503464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173682454-G-A

58503529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173682518-C-T

58503732-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173683159-C-G

58503732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173683159-C-T

58504128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173683516-G-A

58511723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173686454-G-T

58512820-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173687794-G-C

58512887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173687858-G-T

http://identifiers.org/hco/20/GRCh38#58512895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173687866-C-A

58512895-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173687866-C-G

58512936-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173687926-G-C

58513059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173688040-T-C

58513257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173688185-T-C

58513335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173688243-G-T

http://identifiers.org/hco/20/GRCh38#58513472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173688374-C-A

58513522-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173688423-T-A

58513522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173688423-T-C

58513522-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173688423-T-G

58513639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173688525-C-T

58513793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173688681-G-T

http://identifiers.org/hco/20/GRCh38#58514037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173688879-C-A

58514169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173688992-G-A

58514169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173688992-G-T

58514177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173689000-G-A

58514181-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173689004-T-G

58514211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173689038-G-A

58514233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173689051-G-A

58514378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173689178-A-G

58514437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173689224-T-C

58514486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173689272-G-A

58514546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173689334-G-A

58514546-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173689334-G-C

58514546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173689334-G-T

http://identifiers.org/hco/20/GRCh38#58514553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173689341-C-A

58514553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173689341-C-T

http://identifiers.org/hco/20/GRCh38#58514557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173689345-C-A

58514557-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173689345-C-G

58514557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173689345-C-T

58514577-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173689365-G-C

58514577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173689365-G-T

58514682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 173689437-G-A

58514682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 173689437-G-T

58514700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 173689455-G-A

58514700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 173689455-G-T

http://identifiers.org/hco/20/GRCh38#58514718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173689473-C-A

58514718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 173689473-C-T

58514733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 173689484-G-A

58514733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 173689484-G-T

58514784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 173689508-A-G

58514784-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 173689508-A-T

58514808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 173689518-G-A

58514808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 173689518-G-T

http://identifiers.org/hco/20/GRCh38#58514809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173689519-C-A

58514809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 173689519-C-T

58514826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 173689527-A-G

58514829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 173689530-T-C

http://identifiers.org/hco/20/GRCh38#58514849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173689543-C-A

58514849-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 173689543-C-G

58514849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 173689543-C-T

58514889-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 173689577-G-C

58514889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 173689577-G-T

http://identifiers.org/hco/20/GRCh38#58514984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173689647-C-A

58514984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 173689647-C-T

http://identifiers.org/hco/20/GRCh38#58514987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173689650-C-A

58514987-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 173689650-C-G

58514987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 173689650-C-T

58514990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 173689653-G-A

58514990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 173689653-G-T

http://identifiers.org/hco/20/GRCh38#58514996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173689662-C-A

58514996-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 173689662-C-G

58514996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 173689662-C-T

58515023-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 173689689-C-G

58515023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 173689689-C-T

58515039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 173689707-C-T

http://identifiers.org/hco/20/GRCh38#58515066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173689730-C-A

58515066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 173689730-C-T

58515067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 173689731-G-A

58515067-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 173689731-G-C

58515067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 173689731-G-T

58515149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 173689776-G-T

58515211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 173689846-G-A

http://identifiers.org/hco/20/GRCh38#58515284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173689887-C-A

58515287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 173689890-G-T

http://identifiers.org/hco/20/GRCh38#58515330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173689913-C-A

58515330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 173689913-C-T

http://identifiers.org/hco/20/GRCh38#58515331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173689914-C-A

58515331-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 173689914-C-G

58515331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 173689914-C-T

http://identifiers.org/hco/20/GRCh38#58515366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26892
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173689935-C-A