105366932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 52273339-G-A

105366932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 52273339-G-T

http://identifiers.org/hco/3/GRCh38#105366950-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#52273309-A-C

105366950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 52273309-A-G

105367053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 52273194-T-C

105367081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 52273158-G-T

105367086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 52273153-C-T

http://identifiers.org/hco/3/GRCh38#105367098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52273139-C-A

105367098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 52273139-C-T

105367135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 52273102-G-T

http://identifiers.org/hco/3/GRCh38#105367299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52272934-C-A

105367299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 52272934-C-T

105367516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52272711-G-A

105368188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52272094-A-G

http://identifiers.org/hco/3/GRCh38#105368393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52271926-C-A

105368538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52271789-G-T

105368960-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52271362-C-G

105368960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52271362-C-T

105369938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52270451-T-C

105370160-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52270237-A-T

105370280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52270125-A-G

105370728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52269648-G-A

105371149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52269282-C-T

105371154-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52269277-C-G

http://identifiers.org/hco/3/GRCh38#105371157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52269274-C-A

105371157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52269274-C-T

105371258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52269171-T-C

105371295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52269136-T-C

105371376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52269053-T-C

105371407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52269028-G-A

105371739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52268710-G-T

105371972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52268510-A-G

http://identifiers.org/hco/3/GRCh38#105372141-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52268312-A-C

105372308-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52267879-T-A

105372318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52267869-A-G

http://identifiers.org/hco/3/GRCh38#105372578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52267614-C-A

105372796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52267415-C-T

105372816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52267395-T-C

105372856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52267351-C-T

105372921-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52267290-A-T

105372969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52267246-A-G

105373225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52267004-T-C

105373277-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52266951-G-C

105373429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52266821-T-C

105373446-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52266806-T-G

105373478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52266737-G-A

105373486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52266714-T-C

105373641-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52266555-T-G

105373835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52266399-T-C

105373964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52266271-G-A

105376455-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52264844-T-G

105376671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52264666-G-A

105376697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52264640-A-G

105376768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52264575-G-A

105376856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52264486-C-T

105376857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52264485-C-T

105376859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52264483-G-A

105376919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52264424-A-G

105376963-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52264381-T-G

105377073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52264265-A-G

105377193-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52264143-T-G

105377592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52263902-A-G

105377738-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52263737-A-T

http://identifiers.org/hco/3/GRCh38#105377888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52263582-C-A

105377888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52263582-C-T

105381105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52262353-A-G

105381175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52262265-G-A

105381261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52262196-G-A

http://identifiers.org/hco/3/GRCh38#105381313-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52262159-A-C

105381503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52261975-A-G

105381520-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52261958-T-A

105381638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52261838-G-A

105381686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52261797-G-A

105381733-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52261762-T-A

105381733-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52261762-T-G

105381744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52261745-C-T

105381749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52261740-T-C

105382845-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52261683-T-A

105382848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52261680-T-C

105382888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52261643-T-C

105382971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52261564-A-G

http://identifiers.org/hco/3/GRCh38#105383020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52261517-C-A

105383068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52261469-A-G

105383080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52261458-G-T

105383082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52261456-T-C

105383095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52261444-A-G

105383137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52261406-C-T

105383362-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52261184-A-T

105383496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52260946-A-G

105383537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52260904-T-C

105383566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52260882-A-G

105383733-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52260558-A-T

http://identifiers.org/hco/3/GRCh38#105386327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52259977-C-A

105386388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52259930-G-T

105386559-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52259789-C-G

105386721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52259702-A-G

105386740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52259675-T-C

105386861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52259574-A-G

105387032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52259410-G-A

http://identifiers.org/hco/3/GRCh38#105387090-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#52259352-A-C

105387188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52259262-G-A

105387270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52259186-G-A

105387283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52259173-A-G

http://identifiers.org/hco/3/GRCh38#105387385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#52259065-C-A

105387558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52258906-G-A

105387682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52258812-G-A

105387893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52258617-T-C

105388186-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52258191-G-C

105388243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52258130-T-C

105388472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52257926-A-G

105388487-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52257911-C-G

105388771-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52257176-G-C

105388778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52257169-A-G

105388838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52257110-A-G

105388949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52256876-G-A

105389077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52256747-G-A

105389239-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52256554-T-G

105389354-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52256443-A-T

105392955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52256256-A-G

105393265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52255981-A-G

105393434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52255836-G-T

105393601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52255675-C-T

http://identifiers.org/hco/3/GRCh38#105393771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52255505-C-A

105394013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52254146-T-C

105394309-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52253883-C-G

105394338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52253862-A-G

105394443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52253746-C-T

105394507-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52253682-C-G

105395800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52252892-C-T

105395809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52252883-A-G

105395972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52252707-G-A

105396046-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52252634-T-G

105396206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52252520-A-G

105396618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52252145-T-C

105396727-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52252025-G-C

105396829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52251967-A-G

105396878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52251894-A-G

105397478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52251315-T-C

http://identifiers.org/hco/3/GRCh38#105397502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52251305-C-A

http://identifiers.org/hco/3/GRCh38#105397654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52251194-C-A

http://identifiers.org/hco/3/GRCh38#105397779-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52251084-A-C

105397961-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52250912-T-A

105398019-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52250804-T-A

http://identifiers.org/hco/3/GRCh38#105398111-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52250715-A-C

105398140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52250685-T-C

105398395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52250471-G-A

105398424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52250442-A-G

105398854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52250011-G-A

105398986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52249878-G-T

105399517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52249422-A-G

105399573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52249363-T-C

105399623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52249296-C-T

105400030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52248898-T-C

105400159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52248682-G-A

105400255-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52248593-T-G

105400798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52248122-G-A

105409845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52246146-A-G

105409845-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52246146-A-T

105409992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52246015-T-C

http://identifiers.org/hco/3/GRCh38#105410018-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52245989-A-C

105410055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52245955-G-A

http://identifiers.org/hco/3/GRCh38#105410099-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52245913-A-C

105410196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52245827-C-T

105410487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52245575-G-A

105410733-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52245381-C-G

105410962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52245126-C-T

http://identifiers.org/hco/3/GRCh38#105411557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52244317-C-A

105411557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52244317-C-T

105411583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52244291-C-T

105411836-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52244086-G-C

105411839-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52244083-C-G

105412344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52243594-A-G

105412945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52243012-A-G

105412961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52243000-A-G

105413379-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52242611-C-G

105413454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52242536-A-G

105413468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52242522-G-T

105413514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52242476-A-G

105413709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52242278-T-C

105413800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52242188-A-G

105413838-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52242150-C-G

105417028-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52240049-T-A

105417125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52239971-C-T

105417218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52239886-A-G

105417406-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52239678-C-G

105417642-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52239466-T-G

105418597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52238538-T-C

105418721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52238417-A-G

105418751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52238385-G-A

105418808-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52238323-T-A

105418913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52238217-C-T

105418949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52238167-C-T

105418962-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52238154-T-A

105419229-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52237926-C-G

105419255-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52237886-T-A

105419282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52237853-G-A

105419282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52237853-G-T

105419804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52237333-C-T

http://identifiers.org/hco/3/GRCh38#105420043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52237088-C-A

105420655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52234469-G-A

http://identifiers.org/hco/3/GRCh38#105421238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52233900-C-A

105422529-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52233426-G-T

105422681-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52233271-A-T

105422716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52233237-T-C

105422955-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52232998-C-G

105427502-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52230938-T-G

105427731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52230736-T-C

105427845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52230572-A-G

105427938-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52230495-T-A

105427938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52230495-T-C

105428590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52229880-T-C

105428637-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52229837-T-G

105428647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52229831-C-T

105429250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52229225-G-A

105429431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52229018-G-A

105429563-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52228892-C-G

http://identifiers.org/hco/3/GRCh38#105429682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52228771-C-A

105429972-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52228497-T-A

105430386-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52226994-T-G

105430579-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52226813-A-T

105430921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52226288-A-G

105430999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52226209-A-G

105431054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52226149-G-A

105431086-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52226122-T-A

105431086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52226122-T-C

http://identifiers.org/hco/3/GRCh38#105431146-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52226045-A-C

105431156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52226035-A-G

105431185-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52225998-T-A

105431223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52225960-C-T

105431345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52225866-G-A

105431407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52225800-T-C

http://identifiers.org/hco/3/GRCh38#105431471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52225738-C-A

105431567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52225640-C-T

105431594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52225616-C-T

105431621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52225580-A-G

105431800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52225428-G-A

105431851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52225381-G-A

105431851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52225381-G-T

http://identifiers.org/hco/3/GRCh38#105431897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52225345-C-A

http://identifiers.org/hco/3/GRCh38#105432257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52224813-C-A

105432511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52224533-C-T

105432955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52223996-A-G

105432979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52223972-G-A

105433028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52223923-T-C

105433077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52223886-A-G

105433117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52223847-T-C

105433253-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52223699-T-A

105433272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52223680-A-G

http://identifiers.org/hco/3/GRCh38#105433409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52223552-C-A

105433479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52223466-A-G

http://identifiers.org/hco/3/GRCh38#105433951-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52223168-A-C

105434094-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52223005-T-G

http://identifiers.org/hco/3/GRCh38#105434352-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52222739-A-C

105434420-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52222671-A-T

105434428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52222663-C-T

105434954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52222131-C-T

105435032-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52222056-C-G

105435172-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52221969-T-A

105437304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52219905-T-C

105437317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52219892-A-G

105437323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52219883-A-G

105437531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52219451-G-A

105437763-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52219204-G-C

http://identifiers.org/hco/3/GRCh38#105438046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52218888-C-A

105438046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52218888-C-T

105438249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52218596-A-G

105438485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52218335-G-A

105438500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52218320-A-G

105439502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52217170-T-C

105439618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52217054-A-G

105439810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52216883-C-T

http://identifiers.org/hco/3/GRCh38#105439849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52216850-C-A

105440124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52214422-G-A

105440255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52214289-T-C

105440297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52214240-G-A

105440575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52213992-T-C

http://identifiers.org/hco/3/GRCh38#105440833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52213730-C-A

105440863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 52213629-G-T

105440978-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52213509-T-A

105440979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52213508-G-T

105440987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52213500-A-G

105441115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52213369-C-T

105441185-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52213283-A-T

105441341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52213140-T-C

105441386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52213098-C-T

105441529-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52212956-A-T

105441603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52212879-C-T

http://identifiers.org/hco/3/GRCh38#105442102-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52212419-A-C

105442109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52212412-G-T

105442186-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52212344-G-C

105442355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52212172-T-C

105442385-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52212163-T-A

105442385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52212163-T-C

105443170-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52211766-G-C

105443357-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52211595-T-G

105443623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52211337-T-C

105444035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52210959-T-C

105444058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52210927-A-G

http://identifiers.org/hco/3/GRCh38#105444823-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52210547-A-C

http://identifiers.org/hco/3/GRCh38#105444933-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52210422-A-C

105445039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52210313-G-A

105445044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52210292-A-G

105445154-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52210178-T-G

http://identifiers.org/hco/3/GRCh38#105447940-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52209774-A-C

105448051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52209641-C-T

105448339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52208908-G-A

http://identifiers.org/hco/3/GRCh38#105448650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52208613-C-A

105448663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52208600-G-A

105448836-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52208438-A-T

105448858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52208416-A-G

105448868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52208406-C-T

105448906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52208376-G-A

105448906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52208376-G-T

105448953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52208329-A-G

105449004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52208280-A-G

105449163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52208061-A-G

105449334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52207892-G-T

105449504-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52207721-C-G

105449682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52207544-A-G

105450025-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52207216-T-A

105450025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52207216-T-C

105450070-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52207171-C-G

105450090-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52207147-T-G

105450164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52207081-G-A

105450164-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52207081-G-C

105450185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52207070-T-C

105456392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52206722-T-C

105456441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52206674-A-G

105456512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52206605-G-A

105457650-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52206442-A-T

105457845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52206270-T-C

105457971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52206086-A-G

http://identifiers.org/hco/3/GRCh38#105458017-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52205958-A-C

105458039-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52205937-G-C

105458039-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52205937-G-T

105458174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52205753-G-A

105458202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52205733-A-G

105458305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52205643-G-A

105458581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52205345-T-C

105458676-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52205258-C-G

105458792-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52205095-C-G

105458795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52205092-T-C

105458797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52205090-C-T

http://identifiers.org/hco/3/GRCh38#105459343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52205004-C-A

105459682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52204699-C-T

105459760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52204624-C-T

105459767-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52204615-G-C

105459833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52204553-C-T

105459863-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52204529-C-G

105459888-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52204505-G-T

105459942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52204456-G-T

http://identifiers.org/hco/3/GRCh38#105459982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52204421-C-A

105460000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52204403-A-G

105460118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52204289-T-C

105460179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52204228-A-G

105460606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52203809-G-A

105460733-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52203672-T-G

105460762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52203644-G-A

105460862-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52203555-T-A

105460885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52203532-G-A

105460996-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52203439-T-A

105461005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52203430-T-C

105461043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52201444-G-A

105461043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52201444-G-T

105461181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52201317-G-A

105461278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52201244-A-G

105461438-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52201100-A-T

105461602-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52200938-C-G

105461611-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52200931-T-A

105461611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52200931-T-C

http://identifiers.org/hco/3/GRCh38#105461712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52200830-C-A

http://identifiers.org/hco/3/GRCh38#105461863-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52200694-A-C

105461863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52200694-A-G

105461886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52200671-C-T

105461887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52200670-T-C

105461944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52200600-A-G

105461962-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52200582-T-G

105461978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52200566-G-T

105462355-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52200238-G-C

105462483-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52200124-C-G

105462534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52200073-A-G

http://identifiers.org/hco/3/GRCh38#105462549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52200050-C-A

105462575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52200024-C-T

http://identifiers.org/hco/3/GRCh38#105462902-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52199723-A-C

105462902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52199723-A-G

105462931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52199694-A-G

105462938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52199687-C-T

105463017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52199613-C-T

105463247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52199383-A-G

105463505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52199127-C-T

105463617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52199039-A-G

105463713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52198950-C-T

105463735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52198929-A-G

105463760-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52198903-G-C

105463821-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52198832-A-T

105464177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52198486-G-T

105464202-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52198464-A-T

105464383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52198285-T-C

105464517-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52198154-A-T

105464552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52198119-G-A

105464552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52198119-G-T

105465080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52197731-T-C

105465266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52197548-G-A

http://identifiers.org/hco/3/GRCh38#105465272-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52197542-A-C

105465303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52197511-G-A

105465646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52196726-A-G

http://identifiers.org/hco/3/GRCh38#105465696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52196241-C-A

105465750-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52196185-T-A

105465750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52196185-T-C

105465943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52196016-C-T

105466181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52195780-A-G

105466184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52195777-A-G

105466254-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52195707-G-C

105466392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52195570-G-A

105466471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52195500-G-T

105466582-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52195412-T-A

105466717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52195279-A-G

105466739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52195257-C-T

105466841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52195160-T-C

105466906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52195088-C-T

105466963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52195032-A-G

105467152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52194987-G-A

http://identifiers.org/hco/3/GRCh38#105467175-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52194964-A-C

105467218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52194931-T-C

105467298-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52194850-T-G

105467359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52194448-A-G

105467376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52194431-T-C

105467572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52194257-T-C

105467679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52192692-G-A

105467679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52192692-G-T

http://identifiers.org/hco/3/GRCh38#105467724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52192668-C-A

105467858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52192528-A-G

105467898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52192488-A-G

105467989-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52192408-T-G

105468140-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52192244-A-T

105468149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52192235-G-A

105468163-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52192221-G-C

105468199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52192187-T-C

105468506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52191889-A-G

105468685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52191748-A-G

105468741-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52191693-T-A

105468855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52191584-C-T

105468882-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52191554-T-G

105468951-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52191480-T-A

105469079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52191385-A-G

105469092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52191373-T-C

105469184-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52191260-G-C

105469416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52191059-G-A

http://identifiers.org/hco/3/GRCh38#105470508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52186664-C-A

105470508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52186664-C-T

105471066-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52186120-T-A

105471107-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52186083-T-A

http://identifiers.org/hco/3/GRCh38#105471109-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52186081-A-C

105471109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52186081-A-G

105471144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52186047-G-A

105471198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52185991-T-C

105471226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52185963-T-C

105471231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52185958-C-T

105471261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52185945-G-A

105471345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52185858-G-A

105473929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52184829-C-T

105473990-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52184767-T-G

105474123-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52184662-T-G

105474153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52184632-T-C

http://identifiers.org/hco/3/GRCh38#105474612-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52184181-A-C

105474630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52184163-A-G

105474634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52184159-A-G

105474693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52184111-G-T

105474880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52182882-A-G

105474979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52182828-T-C

http://identifiers.org/hco/3/GRCh38#105475092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52182702-C-A

105475499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52182302-T-C

105475661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52182142-T-C

http://identifiers.org/hco/3/GRCh38#105475808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52182021-C-A

105476001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52181848-G-A

105480559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52180036-A-G

105481153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52179433-C-T

105481187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52179400-T-C

105481187-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52179400-T-G

105481295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52179293-A-G

105481336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52179252-C-T

105482056-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52178570-G-C

http://identifiers.org/hco/3/GRCh38#105482151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52178513-C-A

105482151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52178513-C-T

105482465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52178150-G-T

105482556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52178003-A-G

105482737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52177826-T-C

105483186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52177159-T-C

105483281-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52177065-A-T

105483500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52176852-G-A

105483500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52176852-G-T

105483584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52176751-G-A

105483769-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52176112-A-T

105483957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52175937-T-C

105483957-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52175937-T-G

105484032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52175865-G-A

105484406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52175582-A-G

105484570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52175431-C-T

105484630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52175374-C-T

http://identifiers.org/hco/3/GRCh38#105484715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52175289-C-A

http://identifiers.org/hco/3/GRCh38#105484898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52175108-C-A

105484916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52175090-G-A

105485045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52174998-C-T

105485119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52174922-G-A

105485279-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52174766-C-G

105485929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52173994-G-A

105486576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52173342-G-A

105486867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52172720-A-G

105487258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52172315-A-G

105487288-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52172073-A-T

105487389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52171979-A-G

105487609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52171780-A-G

105487629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52171761-C-T

105487649-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52171741-G-C

105487709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52171683-G-A

105487787-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52171574-C-G

105488398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52171427-G-A

105488652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52171250-G-T

105488777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52171209-G-A

105488805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52171177-G-A

105488893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52171093-A-G

105489095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52170647-G-A

105489095-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52170647-G-C

105489279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52170479-G-A

http://identifiers.org/hco/3/GRCh38#105489294-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52170464-A-C

105489412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52170348-A-G

105489425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52170335-T-C

105489514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52170250-A-G

105489812-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52169735-A-T

105490027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52169381-C-T

http://identifiers.org/hco/3/GRCh38#105490179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52169264-C-A

105490250-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52169194-C-G

105490292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52169152-T-C

105490301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52169143-G-A

105490396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52169065-G-A

105492597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52168834-T-C

105492650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52168776-T-C

105492652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52168774-A-G

105492746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52168681-G-T

105492758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52168669-C-T

105492813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52168604-A-G

105493063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52168363-G-T

105493064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52168362-T-C

http://identifiers.org/hco/3/GRCh38#105493506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52167927-C-A

105493506-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52167927-C-G

105493506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52167927-C-T

105493528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52167909-G-A

http://identifiers.org/hco/3/GRCh38#105493555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52167882-C-A

105493555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52167882-C-T

105493576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52167861-A-G

105493751-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52167692-G-C

105493876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52167569-G-A

105494146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52167336-A-G

105494201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52167292-T-C

105494270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52167234-A-G

http://identifiers.org/hco/3/GRCh38#105494336-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52167206-A-C

105494390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52167154-G-T

http://identifiers.org/hco/3/GRCh38#105494492-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52166979-A-C

105494650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52166693-C-T

105494745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52166575-G-A

http://identifiers.org/hco/3/GRCh38#105495075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52166142-C-A

105495075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52166142-C-T

105495103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52166116-C-T

105495104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52166115-G-A

105495111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52166108-T-C

105495163-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52166056-C-G

105495263-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52165968-T-G

105495304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52165928-T-C

105495469-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52165800-T-A

105495472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52165797-G-T

105495532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52165742-A-G

105495720-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52164767-T-G

105495817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52164683-C-T

105495920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52164595-C-T

105496251-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52164278-T-A

105496459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52163832-G-A

105496585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52163708-T-C

105496881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52163418-A-G

105496985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52163316-A-G

105497001-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52163303-T-A

105497177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52163197-T-C

105497314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52163075-C-T

105499803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52160157-C-T

105499804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52160156-T-C

105499816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52160144-A-G

http://identifiers.org/hco/3/GRCh38#105499854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52160106-C-A

http://identifiers.org/hco/3/GRCh38#105499956-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52160003-A-C

105499990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52159959-T-C

105499990-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52159959-T-G

105499999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52159950-T-C

105500106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52159839-C-T

105500118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52159827-T-C

105500560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52157805-T-C

105500644-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52157180-T-G

105500883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52156943-A-G

105501072-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52156751-T-G

105501230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52156596-T-C

105501254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52156568-A-G

105501469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52156376-A-G

105502064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52155643-A-G

105502425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52155020-G-A

105502672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52154773-A-G

105502752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52154696-C-T

http://identifiers.org/hco/3/GRCh38#105503128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52154352-C-A

105503128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52154352-C-T

105503397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52154104-T-C

105503418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52154083-A-G

105503522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52153962-C-T

105503535-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52153944-A-T

105503708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52153775-T-C

105503847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52153644-C-T

105503865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52153627-C-T

105503914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52153578-G-A

105504064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52153419-A-G

105506290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52150160-G-A

105506455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52149940-G-A

105506455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52149940-G-T

105506613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52149802-A-G

105506613-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52149802-A-T

105506827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52149589-A-G

105506959-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52149462-T-G

105507214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52149274-T-C

http://identifiers.org/hco/3/GRCh38#105507386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52149119-C-A

105507456-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52149040-C-G

105507478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52149018-A-G

105507499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52148997-G-A

105507575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52148919-C-T

105507631-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52148868-T-G

105508004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52147278-A-G

105508006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52147276-G-A

105508035-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52147247-T-G

105508266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52147056-T-C

105509418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52145927-G-A

105509669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52145640-A-G

105509799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52145513-A-G

105510029-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52145290-T-G

105510389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52144971-G-A

105510485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52144877-C-T

105510486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52144876-C-T

105510671-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52144698-G-C

105511256-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52144122-T-G

105511309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52144059-C-T

105511511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52143883-C-T

105511880-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52143522-T-G

105511884-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52143518-T-A

105511907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52143497-T-C

105511971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52143433-A-G

105511999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52143405-G-A

105511999-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52143405-G-C

105512103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52143305-G-T

105512498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52142919-G-A

105512643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52142785-A-G

105512717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52142735-A-G

105512788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52142680-A-G

105513301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52142219-A-G

105513309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52142210-A-G

105513334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52142186-A-G

105513353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52142167-C-T

105513437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52142084-T-C

105513465-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52142061-T-A

105513479-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52142047-T-A

105513479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52142047-T-C

105513484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52142032-T-C

105513495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52142000-C-T

105513519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52141976-T-C

105514112-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52139738-A-T

105514121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52139729-G-A

105514145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52139705-C-T

105514246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52139622-C-T

http://identifiers.org/hco/3/GRCh38#105514306-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52139568-A-C

105514398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52139459-G-A

105514621-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52139252-T-G

105514756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52139072-T-C

105514991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52138842-G-A

105515091-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52138740-T-A

105515112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52138724-T-C

105515133-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52138703-T-G

http://identifiers.org/hco/3/GRCh38#105515315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52138433-C-A

105515616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52135932-G-A

105515701-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52135868-T-G

105516496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52135074-C-T

105517008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52134248-A-G

105517100-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52134167-G-C

http://identifiers.org/hco/3/GRCh38#105517338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52133940-C-A

105517384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52133882-T-C

http://identifiers.org/hco/3/GRCh38#105517603-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52133693-A-C

105517603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52133693-A-G

105517603-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52133693-A-T

105517623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52133673-G-A

http://identifiers.org/hco/3/GRCh38#105517928-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52133306-A-C

105517928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52133306-A-G

105517998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52133233-A-G

105518269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52132975-T-C

105518566-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52132167-A-T

105518597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52132134-T-C

105518700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52132029-A-G

105518716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52132013-A-G

105518988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52131668-G-A

105519003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52131653-G-A

105519051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52131600-T-C

105519738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52130607-C-T

105519833-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52130526-G-C

105519982-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52130333-G-C

105519982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52130333-G-T

105519993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52130319-T-C

http://identifiers.org/hco/3/GRCh38#105520007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52130305-C-A

105520007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52130305-C-T

105520041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52130291-T-C

http://identifiers.org/hco/3/GRCh38#105520178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52130162-C-A

105520178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52130162-C-T

http://identifiers.org/hco/3/GRCh38#105520228-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52130062-C-A

105520228-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52130062-C-G

http://identifiers.org/hco/3/GRCh38#105520264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52130034-C-A

105520264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52130034-C-T

105520733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52129578-G-A

105520772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52129539-A-G

105520772-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52129539-A-T

105520774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52129537-G-T

105521334-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52129304-T-A

105521334-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52129304-T-G

105521403-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52129235-G-C

105521727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52128917-A-G

105522436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52128416-A-G

105522582-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52128278-A-T

105522609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52128258-T-C

105522685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52128181-A-G

105522756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52128120-C-T

105523260-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52127929-T-A

http://identifiers.org/hco/3/GRCh38#105523315-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52127868-A-C

105523517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52127629-G-A

105523650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52126802-G-T

105524006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52126439-T-C

105524103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52126346-A-G

105524138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52126289-A-G

105524155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52126272-T-C

105524239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52126186-A-G

105524526-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52125902-G-C

http://identifiers.org/hco/3/GRCh38#105524570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52125861-C-A

105524570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52125861-C-T

105524574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52125857-A-G

105524655-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52125792-T-A

105524658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52125789-A-G

105524666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52125781-A-G

105524681-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52125769-G-C

105524702-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52125750-G-C

105524702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52125750-G-T

105524796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52125669-G-T

105524805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52125659-T-C

105524805-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52125659-T-G

105524836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52125632-G-T

105524861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52125606-T-C

http://identifiers.org/hco/3/GRCh38#105524971-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52125501-A-C

105525029-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52125450-C-G

105525063-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52125414-G-C

105525125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52125371-G-A

105525125-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52125371-G-C

105525484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52125029-T-C

105525526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52124987-T-C

105525573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52124940-G-A

105525594-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52124919-C-G

105525685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52124830-C-T

105525710-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52124805-A-T

105525777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52124738-G-A

105525794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52124721-C-T

105525812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52124703-C-T

105525907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52124611-A-G

105526024-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52124466-T-A

105526167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52124334-G-A

http://identifiers.org/hco/3/GRCh38#105526297-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52124219-A-C

http://identifiers.org/hco/3/GRCh38#105526298-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52124218-A-C

105526783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52123822-G-T

105526880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52123729-C-T

105527360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52123250-G-A

105527445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52123169-T-C

105527939-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52122631-A-T

105528031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52122351-G-A

105528221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52122148-A-G

105528309-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52122060-C-G

http://identifiers.org/hco/3/GRCh38#105528344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52122023-C-A

105528344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52122023-C-T

105528406-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52121979-T-A

105528417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52121968-C-T

105528552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52121840-C-T

105529911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52120162-G-A

105530039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52120047-G-A

105530497-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52119633-C-G

105530497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52119633-C-T

105530837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52119550-T-C

105530953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52119468-T-C

105531052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52119383-G-A

http://identifiers.org/hco/3/GRCh38#105531345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52117996-C-A

http://identifiers.org/hco/3/GRCh38#105531480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52117871-C-A

http://identifiers.org/hco/3/GRCh38#105531518-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52117832-A-C

105531518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52117832-A-G

105531713-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52117637-C-G

105531716-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52117634-T-G

105531763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52117590-G-A

105531894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52117451-G-A

105531894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52117451-G-T

http://identifiers.org/hco/3/GRCh38#105531898-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52117447-A-C

105531898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52117447-A-G

105531919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52117426-G-A

105531919-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52117426-G-C

105531919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52117426-G-T

105532161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52117205-T-C

http://identifiers.org/hco/3/GRCh38#105532199-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52117168-A-C

http://identifiers.org/hco/3/GRCh38#105532230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52117138-C-A

105532632-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52117033-T-A

105532935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52116742-G-T

105534566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52115661-G-A

105534566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52115661-G-T

105534677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 52115553-T-C

105534688-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 52115542-A-T

105534713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 52115517-A-G

105534722-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 52115508-T-G

105534902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52115328-G-T

http://identifiers.org/hco/3/GRCh38#105534921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52115309-C-A

105534921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52115309-C-T

105534953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52115277-G-T

105534973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52115257-G-T

http://identifiers.org/hco/3/GRCh38#105534976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52115254-C-A

105536526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52114911-T-C

105536651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52114785-G-A

105537200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52114321-A-G

105537319-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52114233-A-T

105537546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52114002-A-G

105537997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52113570-A-G

105538001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52113566-G-T

105538400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52113165-G-A

105538609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52112957-C-T

105538632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52112933-C-T

105538723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52112754-G-A

105538723-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52112754-G-C

105538744-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52112731-T-G

105538870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52112614-A-G

105538882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52112602-A-G

105538891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52112593-G-A

105538929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52112517-A-G

105539177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52112294-A-G

http://identifiers.org/hco/3/GRCh38#105539325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52112133-C-A

105539480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52111854-C-T

105539564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52111778-T-C

105539621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52111721-A-G

105539923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52111417-A-G

105539923-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52111417-A-T

105540058-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 52111282-G-C

http://identifiers.org/hco/3/GRCh38#105540113-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52111227-A-C

105540235-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52111064-A-T

105540675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52110666-G-A

105540686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52110655-G-A

http://identifiers.org/hco/3/GRCh38#105540777-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52110597-A-C

105540909-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52110455-T-A

105541028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52110338-G-A

105541323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52109709-G-T

105541399-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52109639-A-T

105541420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52109618-A-G

105541423-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52109615-A-T

105541500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52109547-T-C

http://identifiers.org/hco/3/GRCh38#105541514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52109533-C-A

105541514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52109533-C-T

http://identifiers.org/hco/3/GRCh38#105541521-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52109526-A-C

105541521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52109526-A-G

http://identifiers.org/hco/3/GRCh38#105541539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52109506-C-A

105541539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52109506-C-T

105541553-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52109492-T-A

105541776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52109268-T-C

105541816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52109189-G-A

105541816-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52109189-G-C

105541824-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52109181-T-G

http://identifiers.org/hco/3/GRCh38#105541886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52109127-C-A

105541886-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52109127-C-G

105541886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52109127-C-T

105541894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52109121-A-G

105541903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52109112-A-G

http://identifiers.org/hco/3/GRCh38#105541916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52109097-C-A

105541916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52109097-C-T

105542143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52108731-G-A

105542162-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52108712-A-T

105542163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52108711-C-T

105542241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52108635-G-A

105542276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52108600-T-C

105542278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52108598-T-C

http://identifiers.org/hco/3/GRCh38#105542668-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52100900-A-C

105542668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52100900-A-G

105542701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52100873-T-C

http://identifiers.org/hco/3/GRCh38#105542706-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52100868-A-C

105542924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52100650-T-C

105543034-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52100510-T-G

105543043-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52100501-C-G

105543043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52100501-C-T

105543061-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52100483-T-A

http://identifiers.org/hco/3/GRCh38#105543076-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52100468-A-C

105543226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52100328-G-A

105543226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52100328-G-T

105543422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52100140-T-C

105543422-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52100140-T-G

105543447-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52100122-T-G

105543518-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52100057-C-G

105543518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52100057-C-T

105543527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52100048-T-C

105543676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52099900-C-T

105544178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52098384-T-C

105544344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52098214-T-C

105544348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52098210-G-A

105544386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52098176-A-G

105544392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52098170-G-T

105544393-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52098169-C-G

105544482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52098095-A-G

http://identifiers.org/hco/3/GRCh38#105544491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52098086-C-A

105544503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52098074-T-C

105544521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52098056-G-T

105544538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52098036-G-A

105544538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52098036-G-T

105544585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52097992-G-A

105544585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52097992-G-T

105544592-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52097985-T-A

105544690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52097828-A-G

http://identifiers.org/hco/3/GRCh38#105544786-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52097703-A-C

105544786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52097703-A-G

105544861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52097623-T-C

105544971-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52097518-T-G

105545074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52097416-T-C

http://identifiers.org/hco/3/GRCh38#105545078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52097412-C-A

105545078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52097412-C-T

105545108-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52097383-G-C

105545108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52097383-G-T

http://identifiers.org/hco/3/GRCh38#105545142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52097344-C-A

105545142-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52097344-C-G

105545148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52097338-T-C

105545209-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 52097275-T-G

105545288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 52097196-T-C

105545353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52097129-T-C

http://identifiers.org/hco/3/GRCh38#105545359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52097122-C-A

http://identifiers.org/hco/3/GRCh38#105545360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52097121-C-A

105545369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52097112-G-A

105545374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52097107-G-T

105545470-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52097005-T-G

105545553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52096923-G-A

105545553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52096923-G-T

105546025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52096482-A-G

105546265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52096245-T-C

105547122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52094670-G-T

105547269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 52094523-A-G

105547347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52094446-T-C

http://identifiers.org/hco/3/GRCh38#105547592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52094204-C-A

105547592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52094204-C-T

105547602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52094194-G-T

105547748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52094085-A-G

105547749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52094084-T-C

http://identifiers.org/hco/3/GRCh38#105547763-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52094068-A-C

105547763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52094068-A-G

105548040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52093808-T-C

105548237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52093591-G-A

http://identifiers.org/hco/3/GRCh38#105548395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52093450-C-A

105548772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52093085-G-T

105548824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52093041-T-C

105548929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52092930-A-G

105548961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52092899-G-A

105549181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52092689-A-G

105549459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52092454-G-A

105550030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52091235-G-T

105550193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 52091074-G-A

105550644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52090599-G-A

105550681-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52090562-A-T

105550950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52090305-A-G

105550950-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52090305-A-T

105551252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52090020-G-A

105551318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52089942-C-T

105551393-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52089889-T-A

105551502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52089812-G-A

http://identifiers.org/hco/3/GRCh38#105551518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52089796-C-A

105551518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52089796-C-T

105551755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52089579-G-A

105551792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52089543-T-C

105551855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52089484-T-C

105551896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52089444-T-C

105551916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52089425-T-C

http://identifiers.org/hco/3/GRCh38#105551999-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52089331-A-C

105551999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52089331-A-G

105551999-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52089331-A-T

105552217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52089116-T-C

http://identifiers.org/hco/3/GRCh38#105552270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52089063-C-A

105552270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52089063-C-T

http://identifiers.org/hco/3/GRCh38#105552341-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52088989-C-A

105552341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52088989-C-T

105552518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 52088810-G-A

105552548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 52088780-G-A

105552551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 52088777-G-A

105552551-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 52088777-G-C

105552606-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52088722-C-G

105552606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52088722-C-T

105552618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52088712-T-C

105552722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52088613-A-G

105552756-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52088576-T-G

105552757-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52088575-T-G

105552775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52088557-G-T

105552816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52088522-A-G

105552869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52088462-G-A

http://identifiers.org/hco/3/GRCh38#105552938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52088392-C-A

105552938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52088392-C-T

105552949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52088381-T-C

105553055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52088285-G-A

105553055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52088285-G-T

105553228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52088104-G-T

http://identifiers.org/hco/3/GRCh38#105553245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52088087-C-A

105553245-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52088087-C-G

105553245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52088087-C-T

105553263-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52088068-T-A

http://identifiers.org/hco/3/GRCh38#105553278-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52088053-A-C

http://identifiers.org/hco/3/GRCh38#105553514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52087643-C-A

105553527-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52087630-T-A

105553527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52087630-T-C

105553611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52087550-T-C

105553629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52087541-C-T

105553659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52087513-A-G

105553674-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52087498-A-T

105553827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52087265-G-T

105553878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52087209-G-A

105554017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52087038-C-T

105554057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52086983-G-A

105554078-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52086961-T-A

105554222-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52086795-C-G

105554727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52086322-A-G

http://identifiers.org/hco/3/GRCh38#105555091-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52085973-A-C

105555170-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52085894-A-T

105557377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52085083-G-A

105557625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52084699-A-G

105557658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52084661-A-G

105557692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52084632-T-C

105557697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52084627-A-G

105557699-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52084625-T-G

105557704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52084620-A-G

105557739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52084585-C-T

105557765-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52084555-C-G

105557988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52084364-G-A

105557988-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52084364-G-C

http://identifiers.org/hco/3/GRCh38#105558026-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52084326-A-C

105558225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52084112-C-T

105558443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52083950-C-T

105558450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52083942-G-A

105558548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52083845-G-A

105558631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52083747-T-C

105558711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52083681-G-A

105558734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52083658-C-T

105558896-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52083504-T-A

105558922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52083477-T-C

105559102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52081717-C-T

105559104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52081715-G-A

105559107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52081712-G-A

105559107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52081712-G-T

105565427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52078038-A-G

105565518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52077945-T-C

105565689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52077783-T-C

105565710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52077757-T-C

105565895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52077576-T-C

105565936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52077545-C-T

105566307-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52077248-T-A

105566307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52077248-T-C

105569334-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52076905-T-A

105569450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52076787-A-G

105569558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52076684-T-C

105569653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52076608-G-T

http://identifiers.org/hco/3/GRCh38#105569696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52076568-C-A

105569832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52076431-G-A

105569886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52076380-G-A

105569886-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52076380-G-C

105570084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52076174-G-A

105571688-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52073728-G-C

105571800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52073649-A-G

105571978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52073472-A-G

http://identifiers.org/hco/3/GRCh38#105572010-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52073436-A-C

105572059-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52073383-T-A

105572915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52073256-C-T

105573482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52073016-A-G

105573704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52072776-G-A

105573736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52072750-G-A

105573923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52072566-A-G

105574051-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52072491-C-G

http://identifiers.org/hco/3/GRCh38#105574054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52072488-C-A

105574219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52072319-T-C

105574294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52072188-A-G

105574348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52072141-G-A

105574352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52072137-A-G

105574353-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52072136-T-G

http://identifiers.org/hco/3/GRCh38#105574701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52071783-C-A

105574701-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 52071783-C-G

105575081-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 52071426-C-G

105575160-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 52071345-G-C

http://identifiers.org/hco/3/GRCh38#105575169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52071337-C-A

105575326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 52071166-G-A

105575565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 52070913-A-G

105575569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 52070909-T-C

105575850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 52070606-G-A

105575909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 52070547-G-T

105575950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 3 prime UTR variant
orthologous variants: 52070505-G-A

105575950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 3 prime UTR variant
orthologous variants: 52070505-G-T

http://identifiers.org/hco/3/GRCh38#105576273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52070185-C-A

105576273-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 3 prime UTR variant
orthologous variants: 52070185-C-G

105576513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 3 prime UTR variant
orthologous variants: 52069832-G-A

http://identifiers.org/hco/3/GRCh38#105576592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52069756-C-A

105576658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 3 prime UTR variant
orthologous variants: 52069687-T-C

105576658-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 3 prime UTR variant
orthologous variants: 52069687-T-G

http://identifiers.org/hco/3/GRCh38#105576702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#52069644-C-A

105576702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 3 prime UTR variant
orthologous variants: 52069644-C-T

105576703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 3 prime UTR variant
orthologous variants: 52069643-G-A

105576752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 400
most severe consequence: 3 prime UTR variant
orthologous variants: 52069593-C-T