27970466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: 3 prime UTR variant
orthologous variants: 132451953-C-T

27970513-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: 3 prime UTR variant
orthologous variants: 132451904-T-G

27970581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: 3 prime UTR variant
orthologous variants: 132451837-G-T

27970718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: 3 prime UTR variant
orthologous variants: 132451700-G-T

27970793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: 3 prime UTR variant
orthologous variants: 132451638-A-G

27970842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: 3 prime UTR variant
orthologous variants: 132451601-A-G

http://identifiers.org/hco/1/GRCh38#27970887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132451537-C-A

27970887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: 3 prime UTR variant
orthologous variants: 132451537-C-T

27971138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: 3 prime UTR variant
orthologous variants: 132451299-G-T

27971148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: 3 prime UTR variant
orthologous variants: 132451289-G-A

27971524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: 3 prime UTR variant
orthologous variants: 132450945-G-A

27971524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: 3 prime UTR variant
orthologous variants: 132450945-G-T

http://identifiers.org/hco/1/GRCh38#27971534-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132450935-C-A

27971534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: 3 prime UTR variant
orthologous variants: 132450935-C-T

27971563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: 3 prime UTR variant
orthologous variants: 132450914-C-T

27971793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: 3 prime UTR variant
orthologous variants: 132450810-T-C

27971797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: 3 prime UTR variant
orthologous variants: 132450806-T-C

27971801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: 3 prime UTR variant
orthologous variants: 132450802-G-A

27971805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: 3 prime UTR variant
orthologous variants: 132450798-G-T

http://identifiers.org/hco/1/GRCh38#27971849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132450740-C-A

27971849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: 3 prime UTR variant
orthologous variants: 132450740-C-T

27972003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: 3 prime UTR variant
orthologous variants: 132450653-A-G

27972026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: 3 prime UTR variant
orthologous variants: 132450630-C-T

27972048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: 3 prime UTR variant
orthologous variants: 132450624-G-A

27972048-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: 3 prime UTR variant
orthologous variants: 132450624-G-C

27972196-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: 3 prime UTR variant
orthologous variants: 132450492-C-G

27972252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: 3 prime UTR variant
orthologous variants: 132450438-T-C

27972370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: 3 prime UTR variant
orthologous variants: 132450316-G-T

27972576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: 3 prime UTR variant
orthologous variants: 132450146-T-C

27972580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: 3 prime UTR variant
orthologous variants: 132450142-T-C

27972714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: 3 prime UTR variant
orthologous variants: 132450066-G-A

27972788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: 3 prime UTR variant
orthologous variants: 132449953-G-A

27972811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: 3 prime UTR variant
orthologous variants: 132449930-G-A

27972819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: 3 prime UTR variant
orthologous variants: 132449922-C-T

27973422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: 3 prime UTR variant
orthologous variants: 132449548-G-A

27973422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: 3 prime UTR variant
orthologous variants: 132449548-G-T

http://identifiers.org/hco/1/GRCh38#27973434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132449537-C-A

27973434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: 3 prime UTR variant
orthologous variants: 132449537-C-T

27973659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: 3 prime UTR variant
orthologous variants: 132449319-A-G

27973818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: 3 prime UTR variant
orthologous variants: 132449190-A-G

27973905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: 3 prime UTR variant
orthologous variants: 132449108-A-G

27974048-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: 3 prime UTR variant
orthologous variants: 132448989-T-G

27974365-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: 3 prime UTR variant
orthologous variants: 132448773-C-G

27974365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: 3 prime UTR variant
orthologous variants: 132448773-C-T

27974385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: 3 prime UTR variant
orthologous variants: 132448753-G-A

27974385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: 3 prime UTR variant
orthologous variants: 132448753-G-T

27974407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: 3 prime UTR variant
orthologous variants: 132448731-T-C

27974465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: 3 prime UTR variant
orthologous variants: 132448669-C-T

27974566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron variant
orthologous variants: 132448567-G-T

27974588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron variant
orthologous variants: 132448562-G-A

27974588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron variant
orthologous variants: 132448562-G-T

27974721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron variant
orthologous variants: 132448457-C-T

27978268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron variant
orthologous variants: 132447008-A-G

http://identifiers.org/hco/1/GRCh38#27978283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132446993-C-A

27978283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron variant
orthologous variants: 132446993-C-T

27978298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron variant
orthologous variants: 132446979-A-G

27978492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron variant
orthologous variants: 132446503-T-C

27978602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron variant
orthologous variants: 132446391-G-A

27978602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron variant
orthologous variants: 132446391-G-T

27978606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron variant
orthologous variants: 132446390-G-T

27980704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron variant
orthologous variants: 132440835-C-T

27980956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron variant
orthologous variants: 132440529-C-T

27981008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron variant
orthologous variants: 132440494-A-G

27981374-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron variant
orthologous variants: 132440212-C-G

27981374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron variant
orthologous variants: 132440212-C-T

27988411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron variant
orthologous variants: 132439370-G-A

27988411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron variant
orthologous variants: 132439370-G-T

27988455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron variant
orthologous variants: 132439345-G-T

27988643-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132439164-T-G

27988648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132439159-C-T

http://identifiers.org/hco/1/GRCh38#27988690-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132439113-A-C

27988696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132439107-A-G

27988709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132439095-C-T

27988766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132438961-G-A

27988766-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132438961-G-C

27988766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132438961-G-T

27988919-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132438729-G-C

27989046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132438635-G-A

27989156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132438536-C-T

27989201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132438479-C-T

27989204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132438476-G-A

http://identifiers.org/hco/1/GRCh38#27989620-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132437440-A-C

27989620-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132437440-A-T

27989621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132437439-G-A

27989621-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132437439-G-C

27989621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132437439-G-T

27991110-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132436668-T-G

27991169-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132436615-T-G

27991201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132436597-C-T

27991305-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132436506-T-G

27991321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132436487-A-G

27991419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132436385-T-C

27991536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132436267-A-G

27991536-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132436267-A-T

27993282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132434537-C-T

27993314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132434513-T-C

27993328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132434499-A-G

27993487-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132434345-G-C

http://identifiers.org/hco/1/GRCh38#27993582-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132434250-A-C

27993593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132434233-T-C

27993593-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132434233-T-G

http://identifiers.org/hco/1/GRCh38#27993598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132434228-C-A

27993598-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132434228-C-G

27993598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132434228-C-T

27993641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132434187-G-T

http://identifiers.org/hco/1/GRCh38#27993681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132434125-C-A

27993883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132433840-A-G

27996890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132432183-G-A

27997040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132431974-G-A

http://identifiers.org/hco/1/GRCh38#27997166-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132431848-A-C

http://identifiers.org/hco/1/GRCh38#27997168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132431846-C-A

27997168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132431846-C-T

27997180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132431835-T-C

27997180-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132431835-T-G

http://identifiers.org/hco/1/GRCh38#27997202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132431812-C-A

27997202-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132431812-C-G

27997202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132431812-C-T

27997210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132431804-G-T

27997211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132431803-A-G

27997211-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132431803-A-T

27997279-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132431760-T-A

27997279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132431760-T-C

27997279-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132431760-T-G

27997425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132431614-A-G

27997488-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132431573-T-A

27997504-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132431557-T-A

27997504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132431557-T-C

27998127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132430954-A-G

http://identifiers.org/hco/1/GRCh38#27998174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132430908-C-A

27998258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132430832-G-A

27998258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132430832-G-T

27998273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132430817-G-A

27998394-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132430697-T-A

27998394-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132430697-T-G

27998402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132430689-G-A

27998419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132430672-G-A

27999236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132430395-T-C

http://identifiers.org/hco/1/GRCh38#27999301-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132430335-A-C

28000055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 132428323-A-G

28000083-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132428295-G-C

http://identifiers.org/hco/1/GRCh38#28000095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132428273-C-A

28000097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132428271-T-C

28000129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132428237-A-G

http://identifiers.org/hco/1/GRCh38#28000167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132428211-C-A

28000167-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132428211-C-G

28000167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132428211-C-T

28000182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132428197-G-A

28000182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132428197-G-T

28000197-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132428182-G-C

28000197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132428182-G-T

28000212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132428167-G-A

28000212-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132428167-G-C

28003955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132427232-A-G

28004186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132426872-A-G

http://identifiers.org/hco/1/GRCh38#28004231-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132426843-A-C

28004231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132426843-A-G

28004464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132426297-A-G

28004464-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132426297-A-T

28004488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132426264-A-G

28004528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132426216-A-G

28004947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132425709-G-A

28004948-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132425708-A-T

28005037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132425620-A-G

http://identifiers.org/hco/1/GRCh38#28005106-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132425552-A-C

28010748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132422422-T-C

28011109-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132422031-A-T

28011111-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132422029-G-C

28011149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132421991-A-G

http://identifiers.org/hco/1/GRCh38#28012962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132420581-C-A

28012962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132420581-C-T

28013187-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 132420378-T-A

28013187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 132420378-T-C

28013302-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 132420263-C-G

28017055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132417201-T-C

28017185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132417068-G-A

http://identifiers.org/hco/1/GRCh38#28017317-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132416934-A-C

http://identifiers.org/hco/1/GRCh38#28017353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132416898-C-A

28017353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132416898-C-T

http://identifiers.org/hco/1/GRCh38#28017362-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132416889-C-A

28017362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132416889-C-T

28017511-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132416551-C-G

28017719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132416347-A-G

28017844-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132416043-A-T

28018450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132415821-C-T

28018504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132415785-G-A

28019420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132415350-G-T

28020545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132414838-C-T

28025620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132410287-T-C

28026346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132409905-T-C

28027129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132408843-A-G

28027276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132408727-C-T

28027658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132408317-A-G

http://identifiers.org/hco/1/GRCh38#28027660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132408315-C-A

28027660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132408315-C-T

28028425-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132407615-C-G

28031064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132406761-T-C

28031074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132406751-C-T

28033371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132403568-C-T

28033676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132402879-A-G

28033676-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132402879-A-T

28033683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132402872-C-T

28033691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132402864-G-T

28033802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132402762-C-T

28033942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132402658-C-T

28034585-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132401770-T-A

28034615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132401739-T-C

28035529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132400356-A-G

28035632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 132400253-A-G

28035712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132400172-T-C

28035813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132400074-T-C

28036709-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132399128-T-A

28036739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132399083-A-G

28037303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132398518-T-C

28037312-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132398509-C-G

28037457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132398396-G-A

28037531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132398325-T-C

28037810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132398148-A-G

28037877-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132398083-T-G

28037903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132398059-A-G

28038729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132397636-G-T

28039208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132397183-G-A

28039239-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132397152-G-C

28039731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132396557-C-T

http://identifiers.org/hco/1/GRCh38#28040317-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132396047-A-C

28040446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132395925-G-A

28040930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132395332-G-A

http://identifiers.org/hco/1/GRCh38#28042332-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132394761-A-C

28042609-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132394505-G-C

http://identifiers.org/hco/1/GRCh38#28042697-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132394423-A-C

28042697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132394423-A-G

28042734-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132394385-T-A

28042734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132394385-T-C

28042741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132394378-T-C

28044282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132393290-T-C

28044425-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132393159-C-G

28044633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132392994-T-C

28044808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132392825-G-A

28044808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132392825-G-T

28044838-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132392790-T-A

28045255-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132392217-G-C

http://identifiers.org/hco/1/GRCh38#28045262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132392210-C-A

28045265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132392205-T-C

28045526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132391953-G-A

28045930-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132391603-A-T

28045956-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132391566-C-G

28047969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132389704-G-A

28047994-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132389681-C-G

28048287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132389338-A-G

28048287-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132389338-A-T

28056604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132384956-T-C

28056668-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132384896-G-C

28056773-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132384795-G-C

28056868-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132384708-T-G

28057134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132384449-T-C

28057911-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132384181-G-C

28057911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132384181-G-T

28058031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 132384060-A-G

28058062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 132384030-G-A

28058062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 132384030-G-T

28058063-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 132384029-G-C

28058063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 132384029-G-T

28058998-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132383164-G-C

28059026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132383137-C-T

28059111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132383048-G-A

28059112-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132383047-C-G

28059401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132382778-T-C

28059418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132382761-G-A

28059418-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132382761-G-C

28059495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132382686-C-T

28060104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132382412-C-T

28060157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132382356-T-C

28060281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132382251-C-T

28060673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132381984-C-T

28060929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132381797-G-A

28060929-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132381797-G-C

28061158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132381647-G-A

28061341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132381498-T-C

28061902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132381145-G-A

http://identifiers.org/hco/1/GRCh38#28062641-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132379944-A-C

http://identifiers.org/hco/1/GRCh38#28066541-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132378957-A-C

28066541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132378957-A-G

28066686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132378810-C-T

28070420-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132376493-G-C

28070619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132376338-A-G

28070858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132376126-C-T

28071130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132375923-G-A

28071131-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132375922-C-G

http://identifiers.org/hco/1/GRCh38#28075756-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132374378-A-C

28075756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132374378-A-G

http://identifiers.org/hco/1/GRCh38#28084485-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132370709-A-C

28086143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132369279-C-T

28087273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132367337-G-A

28088359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132366606-G-A

http://identifiers.org/hco/1/GRCh38#28088487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132366501-C-A

28088487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132366501-C-T

http://identifiers.org/hco/1/GRCh38#28088523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132366465-C-A

28088523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 132366465-C-T

http://identifiers.org/hco/1/GRCh38#28088562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#132366427-C-A

28088562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 132366427-C-T

28088564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3521
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 132366425-G-T