http://identifiers.org/hco/16/GRCh38#55509079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93581975-C-A

55509079-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93581975-C-G

55509079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93581975-C-T

55509080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93581976-C-T

55509094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93581990-A-G

55509094-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93581990-A-T

55509127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93582017-T-C

55509138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93582035-G-A

55509138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93582035-G-T

http://identifiers.org/hco/16/GRCh38#55509139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93582036-C-A

55509139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93582036-C-T

http://identifiers.org/hco/16/GRCh38#55509140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#93582037-C-A

55509140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 93582037-C-T

55509164-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93582065-T-A

55509164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93582065-T-C

55509327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 93582228-A-G

55509327-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 93582228-A-T

http://identifiers.org/hco/16/GRCh38#55509350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#93582257-C-A

55509350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, stop_gained, undefined
orthologous variants: 93582257-C-T

55509359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 93582266-G-A

55509359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 93582266-G-T

http://identifiers.org/hco/16/GRCh38#55509420-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93582347-A-C

55509420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93582347-A-G

55509420-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93582347-A-T

55509594-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93582504-T-G

http://identifiers.org/hco/16/GRCh38#55510010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93582803-C-A

55510010-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93582803-C-G

55510010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93582803-C-T

55510012-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93582805-T-G

55510021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93582815-A-G

55510021-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93582815-A-T

55510034-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93582827-T-G

55510077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93582870-G-A

55510427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93583177-A-G

55510427-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93583177-A-T

55510446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93583192-G-A

55510446-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93583192-G-C

55510650-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93583421-T-A

http://identifiers.org/hco/16/GRCh38#55511044-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93583728-A-C

55511495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93584162-G-A

55524612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93588316-G-A

55525011-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93588666-A-T

http://identifiers.org/hco/16/GRCh38#55525179-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93589019-A-C

http://identifiers.org/hco/16/GRCh38#55525377-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93591416-C-A

55525377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93591416-C-T

http://identifiers.org/hco/16/GRCh38#55525391-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93591431-A-C

55525391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93591431-A-G

55525409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93591449-G-A

55525409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93591449-G-T

http://identifiers.org/hco/16/GRCh38#55525418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93591457-C-A

55525433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93591471-A-G

55525511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 93591532-G-A

55525559-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 93591580-T-A

55525637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 93591658-G-T

http://identifiers.org/hco/16/GRCh38#55525990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93592147-C-A

55525995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 93592152-C-T

55526022-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 93592257-C-G

55526022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 93592257-C-T

55526376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron variant
orthologous variants: 93592620-A-G

55526433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron variant
orthologous variants: 93592690-T-C

55526857-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron variant
orthologous variants: 93593150-C-G

55528246-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron variant
orthologous variants: 93596163-T-G

55528283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron variant
orthologous variants: 93596200-G-A

55528283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron variant
orthologous variants: 93596200-G-T

55528410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: synonymous variant
orthologous variants: 93596309-T-C

55528443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: synonymous variant
orthologous variants: 93596342-T-C

http://identifiers.org/hco/16/GRCh38#55528479-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93596378-A-C

http://identifiers.org/hco/16/GRCh38#55528509-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93596408-A-C

55528509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: synonymous variant
orthologous variants: 93596408-A-G

55528566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: synonymous variant
orthologous variants: 93596465-T-C

55528632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron variant
orthologous variants: 93596529-A-G

http://identifiers.org/hco/16/GRCh38#55528637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93596534-C-A

55528637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron variant
orthologous variants: 93596534-C-T

55528846-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron variant
orthologous variants: 93596823-A-T

55528926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron variant
orthologous variants: 93596885-A-G

55529047-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron variant
orthologous variants: 93597021-G-C

55529047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron variant
orthologous variants: 93597021-G-T

55529118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron variant
orthologous variants: 93597092-C-T

55529273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron variant
orthologous variants: 93597263-T-C

55529349-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron variant
orthologous variants: 93597368-T-G

55529351-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron variant
orthologous variants: 93597370-T-A

55529363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron variant
orthologous variants: 93597382-G-A

55529363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron variant
orthologous variants: 93597382-G-T

55529403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron variant
orthologous variants: 93597411-G-A

55529475-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron variant
orthologous variants: 93597472-T-G

55529497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron variant
orthologous variants: 93597481-T-C

55529980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron variant
orthologous variants: 93597911-T-C

55529980-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron variant
orthologous variants: 93597911-T-G

55530004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron variant
orthologous variants: 93597931-G-A

55530028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron variant
orthologous variants: 93597955-A-G

55530057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron variant
orthologous variants: 93597976-A-G

55530059-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron variant
orthologous variants: 93597978-G-C

55530208-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron variant
orthologous variants: 93598099-T-G

55530362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron variant
orthologous variants: 93598177-T-C

55530494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron variant
orthologous variants: 93598312-G-A

55530494-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron variant
orthologous variants: 93598312-G-C

55530494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron variant
orthologous variants: 93598312-G-T

55530505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron variant
orthologous variants: 93598323-A-G

55530506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron variant
orthologous variants: 93598324-C-T

55530839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron variant
orthologous variants: 93598634-A-G

55531023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron variant
orthologous variants: 93598820-A-G

55531039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron variant
orthologous variants: 93598835-C-T

55531305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron variant
orthologous variants: 93599061-T-C

55532008-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron variant
orthologous variants: 93599770-T-A

55532135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 93599918-G-T

http://identifiers.org/hco/16/GRCh38#55532160-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93600037-C-A

55532160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 93600037-C-T

55532213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 93600196-G-T

http://identifiers.org/hco/16/GRCh38#55532228-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93600241-C-A

55532311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 93600322-G-T

55532327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 93600338-A-G

http://identifiers.org/hco/16/GRCh38#55532347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93600365-C-A

55532347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 93600365-C-T

55532363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 93600381-T-C

55532451-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 93600466-G-C

55532487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 93600502-A-G

55532640-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 93600708-T-A

55532640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 93600708-T-C

55532641-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 93600709-T-A

55532641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 93600709-T-C

55532644-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 93600712-T-A

55532711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 93600759-G-A

55532790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 93600826-A-G

55532989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93601000-G-A

55532989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93601000-G-T

55533017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93601032-G-A

55533017-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93601032-G-C

55533017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93601032-G-T

55533110-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93601095-T-G

55533217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93601200-G-T

55533247-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93601230-T-G

55533263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93601245-T-C

55533313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93601288-C-T

55533315-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93601290-G-C

55534143-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93601750-T-A

http://identifiers.org/hco/16/GRCh38#55534253-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93601862-A-C

55534325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93601934-T-C

55534359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93601970-T-C

http://identifiers.org/hco/16/GRCh38#55534362-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93601973-A-C

55534362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93601973-A-G

55534402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93602145-T-C

55534434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93602174-T-C

55534491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93602231-G-A

55534491-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93602231-G-C

55534491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93602231-G-T

55534503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93602243-T-C

55534522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93602260-A-G

55534523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93602261-G-A

55534523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93602261-G-T

55534940-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93602628-G-C

55535016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93602697-A-G

55535071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93602752-G-A

55535125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93602806-G-A

55535125-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93602806-G-C

55535152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93602833-G-A

55535152-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93602833-G-C

55535313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93602971-A-G

55535313-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93602971-A-T

55535843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93603538-G-A

55535920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93603608-T-C

55536008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93603689-G-A

http://identifiers.org/hco/16/GRCh38#55536117-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93603812-A-C

55536124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93603822-A-G

55536133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93603831-A-G

http://identifiers.org/hco/16/GRCh38#55536149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93603847-C-A

55536242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93603915-A-G

55536796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93605229-A-G

http://identifiers.org/hco/16/GRCh38#55536803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93605236-C-A

55537075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93605514-T-C

55537434-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93605899-A-T

55537437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93605902-G-A

55537437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93605902-G-T

55537448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93605913-G-A

55537448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93605913-G-T

55537481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93605946-A-G

55537527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93605975-G-T

55537537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93605984-G-A

http://identifiers.org/hco/16/GRCh38#55537551-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93606002-A-C

http://identifiers.org/hco/16/GRCh38#55537639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93606089-C-A

http://identifiers.org/hco/16/GRCh38#55537727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93606186-C-A

55537727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93606186-C-T

55537788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93606233-A-G

55537905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93606348-T-C

55537955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93606390-G-A

55537955-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93606390-G-C

55538007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93606438-T-C

55538020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93606451-G-T

55538028-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93606459-T-G

55538036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93606467-A-G

55538043-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93606474-T-G

55538069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93606497-A-G

55538131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93606552-G-T

55538154-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93606569-G-C

55538154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93606569-G-T

55538185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93606601-A-G

55538189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93606605-T-C

55538468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93607031-T-C

55538469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93607032-T-C

55538512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93607075-G-T

55538516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93607079-G-A

55538733-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93607275-T-A

55538770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93607320-A-G

55538770-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93607320-A-T

55539019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93607530-T-C

55539074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93607980-C-T

55539103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93608004-A-G

55539162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93608066-T-C

55539227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93608126-C-T

55539234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93608133-G-A

55539234-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93608133-G-C

55539234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93608133-G-T

55539291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93608171-A-G

55539291-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93608171-A-T

http://identifiers.org/hco/16/GRCh38#55539391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93608236-C-A

http://identifiers.org/hco/16/GRCh38#55539714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93608786-C-A

55539733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93608805-G-T

55539769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93608830-G-A

55539796-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93608850-T-G

55539911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93608978-G-A

55541440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93609427-T-C

http://identifiers.org/hco/16/GRCh38#55541560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93609548-C-A

55541576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93609564-T-C

55541576-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93609564-T-G

http://identifiers.org/hco/16/GRCh38#55541609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93609597-C-A

55541628-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93609623-G-C

55541725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93609708-A-G

55541725-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93609708-A-T

http://identifiers.org/hco/16/GRCh38#55541738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93609721-C-A

55541738-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93609721-C-G

55541738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93609721-C-T

55541813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93609785-A-G

http://identifiers.org/hco/16/GRCh38#55541861-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93609832-A-C

55541894-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93609865-C-G

55541941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93609886-G-A

55541941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93609886-G-T

55541947-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93609892-G-C

55541960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93609906-G-A

55541960-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93609906-G-C

55542126-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93610073-T-A

55542126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93610073-T-C

http://identifiers.org/hco/16/GRCh38#55542141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93610093-C-A

55542141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93610093-C-T

55542143-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93610095-T-G

55542159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93610112-T-C

55542170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93610123-G-A

55542170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93610123-G-T

55543527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93610464-T-C

55543677-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93610613-T-G

55543791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93610713-C-T

55543799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93610720-C-T

55543800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93610721-A-G

55543824-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93610745-G-C

55543837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93610758-A-G

55543937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93610830-G-A

55544000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93610892-C-T

55544077-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93610975-C-G

55544095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93611048-G-A

55544289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93611414-G-A

http://identifiers.org/hco/16/GRCh38#55544358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93611498-C-A

http://identifiers.org/hco/16/GRCh38#55544368-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93611508-A-C

55544544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93611741-G-A

55544559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93611756-A-G

55544559-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93611756-A-T

55544671-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93611859-A-T

55544684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93611872-T-C

55544773-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93611967-C-G

55544781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93611975-C-T

55544979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93612147-A-G

55544982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93612150-G-T

55545087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93612244-G-A

55545150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93612604-G-A

55545351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93612840-G-A

55545351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93612840-G-T

55545352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93612841-A-G

55545354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93612843-G-T

55545417-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93612910-G-T

55545515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93613009-T-C

55545515-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93613009-T-G

55545516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93613010-G-A

55545516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93613010-G-T

http://identifiers.org/hco/16/GRCh38#55545594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93613057-C-A

55545594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93613057-C-T

55545630-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93613094-G-C

http://identifiers.org/hco/16/GRCh38#55545680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93613142-C-A

55545681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93613143-A-G

55545721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93613180-T-C

55545772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 93613231-A-G

55545788-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 93613247-T-G

55545838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93613297-A-G

55545937-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93613373-G-C

55545937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93613373-G-T

http://identifiers.org/hco/16/GRCh38#55545947-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93613383-A-C

55545947-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93613383-A-T

55546129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93613519-C-T

55546321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93613743-G-A

55546675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93614917-A-G

55546675-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93614917-A-T

55546689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93614931-A-G

55546722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93614966-T-C

55546778-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93615024-T-A

55546844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93615095-A-G

55547185-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93615124-G-C

55547208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93615147-G-T

55547213-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93615152-G-C

55547332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93615248-C-T

55547384-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93615299-C-G

55547384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93615299-C-T

55547395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93615310-C-T

55547418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93615333-T-C

55547574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93615597-T-C

55549252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93615876-T-C

55549254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93615878-A-G

55549292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 93615916-A-G

55549298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 93615922-A-G

55549393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 93616017-G-A

55549393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 93616017-G-T

55549421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93616045-G-T

http://identifiers.org/hco/16/GRCh38#55549443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93616065-C-A

55549489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93616109-G-T

55549510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93616129-G-A

55549510-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93616129-G-C

55549510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93616129-G-T

http://identifiers.org/hco/16/GRCh38#55549520-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93616139-A-C

55549520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93616139-A-G

55549533-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93616152-T-A

55549533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93616152-T-C

http://identifiers.org/hco/16/GRCh38#55549539-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93616158-A-C

55549539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93616158-A-G

55549539-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93616158-A-T

55549541-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93616160-T-A

55549541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93616160-T-C

55549541-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93616160-T-G

http://identifiers.org/hco/16/GRCh38#55549549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93616168-C-A

55549549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93616168-C-T

55549555-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93616174-A-T

55549638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93616261-G-A

55549669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93616291-G-A

55549786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93616370-A-G

55549790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93616374-T-C

55550359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93616888-A-G

55550374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93616903-A-G

55550434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93616959-G-A

55550437-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93616962-A-T

55550582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93617077-A-G

55550582-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93617077-A-T

55550790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93617154-G-T

55550799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93617163-G-A

55550799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93617163-G-T

55550851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93617211-T-C

55550894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93617254-G-T

http://identifiers.org/hco/16/GRCh38#55550896-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93617256-A-C

55550896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93617256-A-G

55551042-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 93617394-C-G

55551051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 93617403-A-G

http://identifiers.org/hco/16/GRCh38#55551136-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93617486-C-A

55551137-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93617487-T-A

55551155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93617506-T-C

55551285-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93617609-T-A

55551371-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93617630-G-C

55551387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93617646-C-T

55551445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93617686-G-A

55551445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93617686-G-T

55551563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93617803-C-T

55556129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93619224-G-A

55556433-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93620241-T-G

55556957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93620468-A-G

55556974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93620483-G-T

http://identifiers.org/hco/16/GRCh38#55556976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93620485-C-A

55557158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93621671-G-T

55557178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93621687-T-C

55557265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93621738-G-T

55557378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93621835-A-G

55557458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93621915-G-A

55557542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93621989-C-T

55557843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93622132-T-C

55557886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93622166-A-G

55557893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93622173-C-T

55558050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93622317-G-A

55558050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93622317-G-T

55558989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93622978-T-C

55559043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93623017-G-A

55559282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93623241-T-C

55559285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93623244-A-G

55559345-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93623304-C-G

55559345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93623304-C-T

55559422-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93623381-C-G

55559630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93623572-T-C

55559756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93623700-A-G

55559764-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93623708-A-T

55560082-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93623962-A-T

55560251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93624129-G-T

55560376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93624262-G-A

55560548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93624461-A-G

55560598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93624491-G-A

55560800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93624731-T-C

http://identifiers.org/hco/16/GRCh38#55560935-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93624921-A-C

55561075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93625050-G-A

55561075-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93625050-G-C

55561077-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93625052-A-T

55561087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93625063-T-C

55561149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93625115-T-C

55561179-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93625146-T-A

55561227-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93625179-T-G

55561287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93625243-T-C

55561409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93625351-C-T

http://identifiers.org/hco/16/GRCh38#55561412-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93625354-A-C

http://identifiers.org/hco/16/GRCh38#55561561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93625501-C-A

55561561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93625501-C-T

55561757-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93625927-G-C

55561822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93625993-G-T

55561858-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93626031-T-A

55561875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93626048-G-A

55561875-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93626048-G-C

55561948-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93626233-C-G

55561948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93626233-C-T

55562244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93626502-C-T

55562248-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93626506-T-G

55562310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93626560-C-T

http://identifiers.org/hco/16/GRCh38#55562347-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93626596-A-C

55562395-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93626641-T-A

55562439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93626687-G-A

55562447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93626695-G-A

55562578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93626820-G-A

55562770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93627013-G-A

55562793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93627040-A-G

http://identifiers.org/hco/16/GRCh38#55566272-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93627658-A-C

http://identifiers.org/hco/16/GRCh38#55566648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93627998-C-A

55566648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93627998-C-T

http://identifiers.org/hco/16/GRCh38#55566702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93628052-C-A

55566750-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93628106-T-G

55567122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93628475-C-T

55567161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93628514-G-A

55567161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93628514-G-T

http://identifiers.org/hco/16/GRCh38#55567558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93628914-C-A

55567558-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93628914-C-G

http://identifiers.org/hco/16/GRCh38#55567562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93628918-C-A

55567562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93628918-C-T

55567676-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93629029-T-A

55567676-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93629029-T-G

55567707-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93629060-A-T

55567734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93629085-T-C

55567734-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93629085-T-G

55567743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93629094-A-G

55567759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93629110-G-A

55567759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93629110-G-T

http://identifiers.org/hco/16/GRCh38#55568160-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93629320-C-A

55568219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93629375-A-G

55568563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93629700-C-T

55568849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93629971-G-A

55568980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93630105-A-G

55569105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93630220-T-C

55569248-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93630366-T-A

55569299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93630417-T-C

55569386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93630503-A-G

55569458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93630576-G-A

55569504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93630619-A-G

55569587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93630703-A-G

55569612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93630728-G-A

55569612-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93630728-G-C

55569621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93630741-G-A

55569675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93630788-G-A

55569827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93630954-A-G

55569995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93631316-G-A

55571619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93632700-A-G

55572041-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93633077-T-A

55572492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93633397-C-T

55572570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93633471-A-G

55572985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93633637-G-A

55573028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93633674-A-G

55573180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93633826-T-C

55573219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93633856-T-C

55573265-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93633906-C-G

55573551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93633984-G-A

http://identifiers.org/hco/16/GRCh38#55573835-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93634216-A-C

55573841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93634222-C-T

55573888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93635111-T-C

55573914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93635135-A-G

55573946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93635150-G-T

55574006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93635210-A-G

55574047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93635251-G-A

55574479-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93635662-T-A

55574481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93635663-C-T

http://identifiers.org/hco/16/GRCh38#55574489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93635671-C-A

55574489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93635671-C-T

55574660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 93635844-G-A

55574792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93635976-T-C

55574948-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93636129-A-T

55575121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93636284-T-C

55575180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93636336-G-A

55575255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93636411-A-G

55575394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93636535-T-C

55575827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93637051-T-C

http://identifiers.org/hco/16/GRCh38#55576168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93637390-C-A

55576168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93637390-C-T

55576192-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93637414-T-G

55576203-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93637421-A-T

55576433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93637803-T-C

55576826-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93638198-G-C

55577062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93638421-G-A

55577122-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93638492-G-C

55577309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93638949-T-C

55577379-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93639020-A-T

http://identifiers.org/hco/16/GRCh38#55577517-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93639158-A-C

55577859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93639468-G-A

55577951-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93639540-C-G

55578371-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93640178-T-A

55578372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93640179-C-T

55578461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93640238-A-G

55578606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93640359-T-C

55578735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93640455-C-T

http://identifiers.org/hco/16/GRCh38#55578880-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93640599-C-A

55578973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93640700-A-G

55578975-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93640702-G-C

55578975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93640702-G-T

http://identifiers.org/hco/16/GRCh38#55578979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93640706-C-A

55578979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93640706-C-T

55579024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93640788-G-T

55579025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93640789-A-G

55579025-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93640789-A-T

http://identifiers.org/hco/16/GRCh38#55579037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93640801-C-A

55579037-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93640801-C-G

55579037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93640801-C-T

55579052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93640816-T-C

55579256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93641020-A-G

55579256-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93641020-A-T

55579285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93641041-G-A

55579285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93641041-G-T

55579300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93641056-G-A

55579313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93641071-A-G

55579322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93641080-T-C

55579356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93641100-A-G

55579376-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93641120-A-T

55579377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93641121-G-A

55579377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93641121-G-T

55579381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93641125-T-C

55579719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93641432-A-G

55579760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93641473-T-C

http://identifiers.org/hco/16/GRCh38#55580096-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93642035-A-C

55580170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93642115-G-A

55580186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93642131-T-C

55581106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93643296-A-G

55581877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93643688-C-T

55582132-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93643921-T-G

55582179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93643994-A-G

55582248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93644062-C-T

55582398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93644168-T-C

55582460-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93644229-A-T

55582574-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93644321-A-T

http://identifiers.org/hco/16/GRCh38#55582760-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93644512-A-C

55582780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93644532-T-C

55582837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93644588-A-G

55582837-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93644588-A-T

http://identifiers.org/hco/16/GRCh38#55582857-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93644608-A-C

55582857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93644608-A-G

55583092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 93644841-T-C

http://identifiers.org/hco/16/GRCh38#55583137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93644870-C-A

55583137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93644870-C-T

55583144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93644877-T-C

55583237-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93644977-T-A

55583300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93645022-G-A

55583300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93645022-G-T

55583316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93645038-T-C

55583316-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93645038-T-G

55583420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93645159-G-A

55583420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93645159-G-T

http://identifiers.org/hco/16/GRCh38#55583476-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93645205-A-C

55583476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93645205-A-G

55583484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93645212-A-G

http://identifiers.org/hco/16/GRCh38#55583496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93645224-C-A

http://identifiers.org/hco/16/GRCh38#55583652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93645354-C-A

55583652-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93645354-C-G

55584015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93645374-A-G

55584149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93645509-G-T

http://identifiers.org/hco/16/GRCh38#55584179-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93645539-A-C

http://identifiers.org/hco/16/GRCh38#55584251-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93645612-A-C

55584286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93645655-T-C

http://identifiers.org/hco/16/GRCh38#55584710-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93646044-A-C

55585550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93646280-A-G

55585552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93646282-T-C

55585574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93646304-G-A

55585613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93646351-A-G

http://identifiers.org/hco/16/GRCh38#55585778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93646829-C-A

55585864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93646909-T-C

55585996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93647021-A-G

55586171-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93647571-T-G

55586196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93647596-T-C

http://identifiers.org/hco/16/GRCh38#55586347-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93647750-A-C

55586347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93647750-A-G

55586347-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93647750-A-T

55586353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93647756-G-T

http://identifiers.org/hco/16/GRCh38#55586548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93648026-C-A

55586548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93648026-C-T

http://identifiers.org/hco/16/GRCh38#55586585-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93648064-A-C

55586599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93648078-G-T

55586602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93648081-T-C

55586621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93648100-G-A

55586626-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93648108-G-C

55586626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93648108-G-T

http://identifiers.org/hco/16/GRCh38#55586637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26032
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93648119-C-A