http://identifiers.org/hco/8/GRCh38#94487925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11550466-C-A

94487925-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: 3 prime UTR variant
orthologous variants: 11550466-C-G

94488093-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: 3 prime UTR variant
orthologous variants: 11550319-T-G

http://identifiers.org/hco/8/GRCh38#94488211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11550205-C-A

94488671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 11549730-G-A

http://identifiers.org/hco/8/GRCh38#94488782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11549621-C-A

94489206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11549106-T-C

94489393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11548972-G-A

94489393-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11548972-G-C

http://identifiers.org/hco/8/GRCh38#94490097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11548714-C-A

94490097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11548714-C-T

http://identifiers.org/hco/8/GRCh38#94490109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11548707-C-A

94490109-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11548707-C-G

94490166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11548512-A-G

94490617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11548206-T-C

94490617-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11548206-T-G

94490698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11548091-T-C

94490792-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11547987-A-T

94490801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11547982-T-C

94491512-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11546353-A-T

94491569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11546307-A-G

94491977-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11545886-T-G

94492017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11545826-G-A

94492017-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11545826-G-C

94492017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11545826-G-T

94492615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11545031-T-C

http://identifiers.org/hco/8/GRCh38#94492854-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11544795-A-C

94492913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11544744-G-A

94492913-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11544744-G-C

94492913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11544744-G-T

94493149-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11544521-A-T

94493567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11543174-A-G

94493741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11542999-T-C

94493838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11542868-G-A

94493866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11542840-C-T

http://identifiers.org/hco/8/GRCh38#94494415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11542474-C-A

94494578-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11542443-T-A

94494578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11542443-T-C

94494578-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11542443-T-G

94494635-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11542430-T-A

94494665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11542400-G-A

http://identifiers.org/hco/8/GRCh38#94494724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11542337-C-A

94494724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11542337-C-T

94494770-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11542295-T-G

94494801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11542264-T-C

94494924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 11542137-T-C

94494948-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 11542113-T-A

94494948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 11542113-T-C

94494949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 11542112-A-G

94494961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 11542100-A-G

94494961-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 11542100-A-T

http://identifiers.org/hco/8/GRCh38#94494975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11542084-C-A

94494975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11542084-C-T

94495600-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11540769-C-G

94495600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11540769-C-T

94495614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11540753-A-G

94495647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11540725-G-A

94495647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11540725-G-T

http://identifiers.org/hco/8/GRCh38#94495654-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11540718-A-C

94495654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11540718-A-G

http://identifiers.org/hco/8/GRCh38#94495716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11540654-C-A

94495716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11540654-C-T

94495923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11540449-G-A

94495923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11540449-G-T

94495997-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11540367-T-A

94495997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11540367-T-C

94496018-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11540344-T-A

94496018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11540344-T-C

http://identifiers.org/hco/8/GRCh38#94496096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11540271-C-A

94496096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11540271-C-T

http://identifiers.org/hco/8/GRCh38#94496258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11540131-C-A

94496258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11540131-C-T

94496266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11540123-T-C

94496529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11539861-A-G

94496553-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11539838-T-A

94496667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11539577-T-C

94496754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11539465-T-C

http://identifiers.org/hco/8/GRCh38#94499432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11534261-C-A

94499432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11534261-C-T

94499521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11534172-A-G

94499521-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11534172-A-T

94506392-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11531128-T-A

94506392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11531128-T-C

http://identifiers.org/hco/8/GRCh38#94506398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11531122-C-A

http://identifiers.org/hco/8/GRCh38#94506411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11531109-C-A

94506411-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11531109-C-G

94506429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11531086-G-A

94506429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11531086-G-T

94506515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11531028-A-G

94506524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11531019-T-C

94506533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11531010-G-T

94506548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11530995-G-T

94506591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11530952-T-C

94506599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11530944-G-A

http://identifiers.org/hco/8/GRCh38#94506790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11530770-C-A

94506790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11530770-C-T

http://identifiers.org/hco/8/GRCh38#94506819-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11530741-A-C

94508697-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11529583-T-A

94508697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11529583-T-C

94508727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11529570-C-T

94509015-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11529332-A-T

94509533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11528978-C-T

94509596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11528891-C-T

http://identifiers.org/hco/8/GRCh38#94509631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11528847-C-A

94509631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11528847-C-T

94510059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11528429-C-T

94510307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11527990-G-T

94510716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11527587-C-T

94511057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11527258-C-T

94511106-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11527213-G-C

94511106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11527213-G-T

http://identifiers.org/hco/8/GRCh38#94511282-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11527040-A-C

94511282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11527040-A-G

94511309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11527013-T-C

94511360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11526962-G-A

http://identifiers.org/hco/8/GRCh38#94511638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11526684-C-A

94511638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11526684-C-T

94512001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11526433-A-G

94512001-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11526433-A-T

94512830-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11525156-G-C

94512946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11525071-T-C

94513417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11524782-G-A

94513417-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11524782-G-T

94513437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11524759-A-G

94513881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11523856-C-T

94513966-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11523776-G-C

94514003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11523738-G-A

94514088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11523665-C-T

http://identifiers.org/hco/8/GRCh38#94514842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11522958-C-A

94514842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11522958-C-T

94514843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11522957-A-G

94514870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, missense_variant, splice_region_variant
orthologous variants: 11522932-T-C

94514870-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, missense_variant, splice_region_variant
orthologous variants: 11522932-T-G

http://identifiers.org/hco/8/GRCh38#94514993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11522808-C-A

94514993-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11522808-C-G

94514993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11522808-C-T

94515042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11522770-G-T

94515099-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11522711-T-A

94515099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11522711-T-C

http://identifiers.org/hco/8/GRCh38#94515725-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11522528-A-C

http://identifiers.org/hco/8/GRCh38#94516208-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11522369-A-C

94517722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11521322-T-C

http://identifiers.org/hco/8/GRCh38#94517748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11521298-C-A

94517748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11521298-C-T

94517769-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11521276-A-T

http://identifiers.org/hco/8/GRCh38#94517823-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11521222-A-C

http://identifiers.org/hco/8/GRCh38#94517863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11521182-C-A

94517892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 11521153-A-G

94517897-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 11521148-T-A

94517904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 11521141-G-A

http://identifiers.org/hco/8/GRCh38#94517953-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11521092-A-C

94517953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11521092-A-G

94517969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11521079-T-C

94517970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11521078-T-C

94517974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11521074-T-C

94517978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11521070-A-G

http://identifiers.org/hco/8/GRCh38#94517983-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11521065-A-C

94517983-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11521065-A-T

94517992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11521056-G-A

94517992-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11521056-G-C

http://identifiers.org/hco/8/GRCh38#94518006-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11521042-A-C

http://identifiers.org/hco/8/GRCh38#94518019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11521029-C-A

94518031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11521019-G-T

http://identifiers.org/hco/8/GRCh38#94518397-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11520053-A-C

94518614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11519822-A-G

94518732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11519724-G-A

http://identifiers.org/hco/8/GRCh38#94518958-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11519439-A-C

94518958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11519439-A-G

http://identifiers.org/hco/8/GRCh38#94518985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, missense_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11519412-C-A

94518985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, missense_variant, splice_region_variant
orthologous variants: 11519412-C-T

94519156-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 11519241-C-G

94519234-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 11519163-T-A

94519507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11518895-T-C

94519614-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11518791-A-T

94519678-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11518744-G-C

94519678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11518744-G-T

94519827-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11518617-T-A

94519827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11518617-T-C

94522060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11516411-G-A

94522157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11516338-T-C

94522448-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11516080-T-A

94522448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11516080-T-C

94522461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11516067-C-T

94522989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11515564-T-C

http://identifiers.org/hco/8/GRCh38#94523072-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11515425-A-C

94523135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11515366-T-C

94523136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11515365-G-T

94523260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11515093-T-C

94523276-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11515077-T-G

94525772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11514569-G-A

94525817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11514545-G-A

94526097-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11514282-T-A

94526097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11514282-T-C

94526097-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11514282-T-G

94526174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11514206-T-C

94526182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11514198-G-T

94526215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 11514174-T-C

94526467-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: missense variant
orthologous variants: 11513922-C-G

94526467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: missense variant
orthologous variants: 11513922-C-T

94526601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: missense variant
orthologous variants: 11513788-G-A

94526763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: missense variant
orthologous variants: 11513626-T-C

94526972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: synonymous variant
orthologous variants: 11513417-T-C

94526999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: synonymous variant
orthologous variants: 11513390-T-C

94527063-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: missense variant
orthologous variants: 11513326-T-A

94527107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: synonymous variant
orthologous variants: 11513282-G-A

94527107-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: missense variant
orthologous variants: 11513282-G-C

94527243-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 11513146-G-C

http://identifiers.org/hco/8/GRCh38#94527336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11513053-C-A

94527397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron variant
orthologous variants: 11512992-C-T

http://identifiers.org/hco/8/GRCh38#94527423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11512968-C-A

94527423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron variant
orthologous variants: 11512968-C-T

http://identifiers.org/hco/8/GRCh38#94527469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11512902-C-A

94527469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron variant
orthologous variants: 11512902-C-T

94527497-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron variant
orthologous variants: 11512869-T-A

94527497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron variant
orthologous variants: 11512869-T-C

94527717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron variant
orthologous variants: 11512709-G-T

94528322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron variant
orthologous variants: 11509043-T-C

94528883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron_variant, undefined
orthologous variants: 11508379-G-A

http://identifiers.org/hco/8/GRCh38#94528940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#11508302-C-A

94528943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron_variant, undefined
orthologous variants: 11508299-G-A

94528943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron_variant, undefined
orthologous variants: 11508299-G-T

94528947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron_variant, undefined
orthologous variants: 11508295-C-T

94528969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron_variant, undefined
orthologous variants: 11508279-G-T

94529111-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 11508136-T-A

94529217-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11508030-G-C

94529217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11508030-G-T

94529308-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11507939-T-G

http://identifiers.org/hco/8/GRCh38#94529416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11507826-C-A

94529416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11507826-C-T

94529417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11507825-A-G

94529424-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11507818-T-A

94529424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11507818-T-C

94530771-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11507266-G-C

http://identifiers.org/hco/8/GRCh38#94530869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11507176-C-A

94530869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11507176-C-T

94530917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11507124-T-C

94530930-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11507103-G-C

94530930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11507103-G-T

94533089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11506364-T-C

94533167-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11506290-T-A

94533231-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11506215-T-G

94533253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11506192-A-G

94535048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11505403-G-A

94535067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11505384-T-C

94535071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11505380-T-C

94535143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11504713-G-T

94535156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11504698-G-T

http://identifiers.org/hco/8/GRCh38#94535222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11504641-C-A

94535230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11504632-C-T

94535254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11504608-C-T

94537059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11501402-G-A

94537059-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11501402-G-C

94537059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11501402-G-T

94537194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11501263-A-G

94538029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11499031-C-T

94542093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11496899-G-A

94542097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11496895-C-T

94542221-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11496796-A-T

94542705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11495317-G-A

94543801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11494898-T-C

http://identifiers.org/hco/8/GRCh38#94544026-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11494685-A-C

94544026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron variant
orthologous variants: 11494685-A-G

http://identifiers.org/hco/8/GRCh38#94546084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11492887-C-A

94546116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron variant
orthologous variants: 11492856-T-C

94546144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron variant
orthologous variants: 11492829-G-A

94546222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron variant
orthologous variants: 11492752-T-C

94546286-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron variant
orthologous variants: 11492713-T-A

94546437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron variant
orthologous variants: 11492563-G-A

94546458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron variant
orthologous variants: 11492536-C-T

http://identifiers.org/hco/8/GRCh38#94546969-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11492264-A-C

94547086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron variant
orthologous variants: 11492161-G-A

94547086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron variant
orthologous variants: 11492161-G-T

94547117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron variant
orthologous variants: 11492130-T-C

94547281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron variant
orthologous variants: 11491825-G-A

94547357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron variant
orthologous variants: 11491740-T-C

94548081-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron variant
orthologous variants: 11491189-T-A

94548081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron variant
orthologous variants: 11491189-T-C

94551029-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron variant
orthologous variants: 11488539-T-G

94551348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron variant
orthologous variants: 11487862-C-T

94551354-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron variant
orthologous variants: 11487856-T-G

http://identifiers.org/hco/8/GRCh38#94551479-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11487785-A-C

94551531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron variant
orthologous variants: 11487745-G-A

94551808-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron variant
orthologous variants: 11487505-T-G

94552075-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron variant
orthologous variants: 11487378-A-T

94552078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron variant
orthologous variants: 11487375-A-G

94552602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron variant
orthologous variants: 11486805-T-C

http://identifiers.org/hco/8/GRCh38#94553244-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#11486245-A-C

http://identifiers.org/hco/8/GRCh38#94553345-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11486143-A-C

94553359-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron_variant, undefined
orthologous variants: 11486129-G-C

94553359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: intron_variant, undefined
orthologous variants: 11486129-G-T

94553504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 11485985-G-A

94553504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 11485985-G-T

94553515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: 5 prime UTR variant
orthologous variants: 11485974-T-C

http://identifiers.org/hco/8/GRCh38#94553516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11485973-C-A

94553516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24500
most severe consequence: 5 prime UTR variant
orthologous variants: 11485973-C-T