http://identifiers.org/hco/1/GRCh38#944216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156332130-C-A

944216-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 156332130-C-G

944216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 156332130-C-T

944222-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 156332124-T-A

944222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 156332124-T-C

http://identifiers.org/hco/1/GRCh38#944258-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156332085-A-C

944268-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 156332073-T-A

944268-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 156332073-T-G

944277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 156332061-A-G

944279-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 156332059-T-A

944279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 156332059-T-C

944279-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 156332059-T-G

http://identifiers.org/hco/1/GRCh38#944283-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156332055-A-C

944283-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 156332055-A-T

944291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 156332046-G-A

944291-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 156332046-G-C

944291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 156332046-G-T

944307-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 156332005-T-A

944307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 156332005-T-C

944307-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 156332005-T-G

944311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 156332001-A-G

http://identifiers.org/hco/1/GRCh38#944314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156331998-C-A

944314-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 156331998-C-G

944314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 156331998-C-T

http://identifiers.org/hco/1/GRCh38#944327-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156331986-A-C

944327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 156331986-A-G

944327-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 156331986-A-T

944344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 156331932-G-A

944344-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 156331932-G-C

944344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 156331932-G-T

944352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 156331924-A-G

944357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 156331830-T-C

944357-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 156331830-T-G

944358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 156331829-G-A

944358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 156331829-G-T

944373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 156331810-A-G

944373-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 156331810-A-T

http://identifiers.org/hco/1/GRCh38#944396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156331787-C-A

944396-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 156331787-C-G

944471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 156331744-T-C

944471-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 156331744-T-G

944477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 156331738-G-A

944477-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 156331738-G-C

944477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 156331738-G-T

http://identifiers.org/hco/1/GRCh38#944516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156331698-C-A

944516-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 156331698-C-G

944516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 156331698-C-T

944527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 156331682-T-C

944527-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 156331682-T-G

944529-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 156331680-T-A

944529-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 156331680-T-G

http://identifiers.org/hco/1/GRCh38#944568-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156331646-A-C

944568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 156331646-A-G

http://identifiers.org/hco/1/GRCh38#944577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156331637-C-A

944577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 156331637-C-T

944579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 156331635-G-A

944579-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 156331635-G-C

944579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 156331635-G-T

944580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 156331634-T-C

http://identifiers.org/hco/1/GRCh38#944598-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156331618-A-C

944598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 156331618-A-G

http://identifiers.org/hco/1/GRCh38#944608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156331608-C-A

944608-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 156331608-C-G

944608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 156331608-C-T

944616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 156331603-T-C

http://identifiers.org/hco/1/GRCh38#944630-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156331594-C-A

944630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 156331594-C-T

944736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 156331532-C-T

944782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156331492-T-C

944809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156331465-A-G

944886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156331385-G-A

944886-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156331385-G-C

944886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156331385-G-T

http://identifiers.org/hco/1/GRCh38#944904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156331361-C-A

944904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156331361-C-T

944940-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156331323-G-C

944951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156331313-G-A

945035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 156331240-C-T

945102-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156331176-C-G

945111-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156331167-C-G

945128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156331150-C-T

945147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 156331131-C-T

945148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 156331130-T-C

945164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156331115-G-A

945169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156331110-C-T

http://identifiers.org/hco/1/GRCh38#945183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156331063-C-A

945184-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156331062-C-G

945184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156331062-C-T

945191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156331055-T-C

945213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156331021-G-A

945213-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156331021-G-C

945213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156331021-G-T

945277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156330910-G-A

945277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156330910-G-T

945295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156330880-G-A

945295-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156330880-G-C

945298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156330877-G-T

http://identifiers.org/hco/1/GRCh38#945300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156330869-C-A

945313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156330856-A-G

945315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156330854-A-G

http://identifiers.org/hco/1/GRCh38#945330-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156330841-A-C

945330-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156330841-A-T

945344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156330815-T-C

945344-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156330815-T-G

http://identifiers.org/hco/1/GRCh38#945345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156330814-C-A

945345-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156330814-C-G

945345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156330814-C-T

945356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156330809-G-A

945356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156330809-G-T

945377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156330789-G-A

945377-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156330789-G-C

945377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156330789-G-T

945390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156330776-T-C

945403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156330759-G-A

945403-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156330759-G-C

945403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156330759-G-T

945404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156330758-C-T

945413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156330749-G-A

945413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156330749-G-T

945432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156330721-G-A

945432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156330721-G-T

945433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156330720-G-A

945433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156330720-G-T

945454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156330628-T-C

945486-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156330586-C-G

945486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156330586-C-T

http://identifiers.org/hco/1/GRCh38#945532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156330407-C-A

945532-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156330407-C-G

945532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156330407-C-T

945541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156330398-T-C

945613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156330326-A-G

945661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 156330278-G-A

945665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156330274-A-G

945719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156330224-A-G

945723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156330220-A-G

945723-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156330220-A-T

945852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156330199-T-C

945943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156330151-G-A

945946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156330148-G-A

http://identifiers.org/hco/1/GRCh38#946056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156330071-C-A

946056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156330071-C-T

946062-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156330065-T-G

http://identifiers.org/hco/1/GRCh38#946082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156330054-C-A

946082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156330054-C-T

946104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156330032-G-A

946104-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156330032-G-C

946104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156330032-G-T

946164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156330007-G-A

946164-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156330007-G-C

946164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156330007-G-T

http://identifiers.org/hco/1/GRCh38#946332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156329841-C-A

946332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156329841-C-T

946342-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156329831-T-G

946361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156329817-G-A

http://identifiers.org/hco/1/GRCh38#946369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156329809-C-A

946369-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156329809-C-G

946369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156329809-C-T

946393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156329774-C-T

946410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 156329757-G-A

946410-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156329757-G-C

946429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 156329738-G-A

946429-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 156329738-G-C

946430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156329737-G-A

946437-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 156329730-T-G

946445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156329722-C-T

946450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 156329717-G-A

946454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156329713-A-G

946457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156329710-T-C

946458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156329709-A-G

946463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156329704-G-A

946463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 156329704-G-T

946511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156329656-T-C

947154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156329441-C-T

947156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156329439-T-C

947157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156329438-A-G

947231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156329330-C-T

947286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156329274-A-G

947434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156329155-T-C

947474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156329128-G-A

947474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156329128-G-T

947518-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156329084-C-G

http://identifiers.org/hco/1/GRCh38#948069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156328687-C-A

948069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156328687-C-T

948087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156328669-G-T

948118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156328629-G-A

948118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156328629-G-T

948136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156328591-G-T

http://identifiers.org/hco/1/GRCh38#948146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156328581-C-A

http://identifiers.org/hco/1/GRCh38#948171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156328556-C-A

948171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156328556-C-T

948199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 156328528-G-A

948199-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156328528-G-C

948199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156328528-G-T

http://identifiers.org/hco/1/GRCh38#948208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156328519-C-A

948208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156328519-C-T

948225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156328502-A-G

http://identifiers.org/hco/1/GRCh38#948228-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156328499-C-A

948228-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156328499-C-G

948228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156328499-C-T

http://identifiers.org/hco/1/GRCh38#948293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156328429-C-A

948293-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156328429-C-G

948293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156328429-C-T

http://identifiers.org/hco/1/GRCh38#948338-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156328350-A-C

http://identifiers.org/hco/1/GRCh38#948339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156328349-C-A

948339-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156328349-C-G

948339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156328349-C-T

http://identifiers.org/hco/1/GRCh38#948343-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156328345-A-C

948343-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156328345-A-T

948345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156328343-G-T

948351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156328337-G-T

948360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156328322-G-A

948360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156328322-G-T

948370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156328281-T-C

948370-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156328281-T-G

948395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156328236-G-A

948395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156328236-G-T

http://identifiers.org/hco/1/GRCh38#948428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156328159-C-A

948432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156328155-G-A

948432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156328155-G-T

948468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156328107-C-T

948475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156328093-G-A

948479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156328089-G-A

948479-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156328089-G-C

948479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156328089-G-T

948557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156328011-G-A

948557-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156328011-G-C

http://identifiers.org/hco/1/GRCh38#951107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156327146-C-A

951107-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156327146-C-G

951107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156327146-C-T

http://identifiers.org/hco/1/GRCh38#951108-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156327145-C-A

951128-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 156327131-T-A

951143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156327116-A-G

951143-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156327116-A-T

951258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156326995-G-A

951258-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156326995-G-C

951258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156326995-G-T

951283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156326973-G-T

951285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156326971-C-T

951295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156326961-C-T

951311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156326949-A-G

http://identifiers.org/hco/1/GRCh38#951316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156326945-C-A

http://identifiers.org/hco/1/GRCh38#951321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156326935-C-A

951321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156326935-C-T

http://identifiers.org/hco/1/GRCh38#951332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156326924-C-A

http://identifiers.org/hco/1/GRCh38#951340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156326904-C-A

951340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156326904-C-T

http://identifiers.org/hco/1/GRCh38#951354-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156326885-A-C

951354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156326885-A-G

951408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156326784-G-A

951483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156326728-T-C

951488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156326723-G-A

http://identifiers.org/hco/1/GRCh38#951527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156326683-C-A

951530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156326680-A-G

951533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156326677-C-T

951634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156326599-C-T

951696-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156326547-C-G

http://identifiers.org/hco/1/GRCh38#951709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156326542-C-A

http://identifiers.org/hco/1/GRCh38#951749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156326494-C-A

951749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156326494-C-T

951777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156326488-C-T

951785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156326480-G-A

http://identifiers.org/hco/1/GRCh38#951973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156326278-C-A

951973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156326278-C-T

951979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156326272-C-T

951980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156326271-C-T

952021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156326234-T-C

952039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156326216-A-G

952131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 156326124-G-A

952131-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 156326124-G-C

952149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156326106-G-A

952156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156326098-A-G

http://identifiers.org/hco/1/GRCh38#952157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156326097-C-A

952157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156326097-C-T

952252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156326068-C-T

http://identifiers.org/hco/1/GRCh38#952258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156326062-C-A

952258-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156326062-C-G

952258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156326062-C-T

http://identifiers.org/hco/1/GRCh38#952262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156326058-C-A

952262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156326058-C-T

http://identifiers.org/hco/1/GRCh38#952268-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156326052-C-A

952268-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156326052-C-G

952320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156326018-C-T

952321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156326017-T-C

http://identifiers.org/hco/1/GRCh38#952323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156326015-C-A

952323-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156326015-C-G

952323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156326015-C-T

952327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156326011-G-A

http://identifiers.org/hco/1/GRCh38#952357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156325987-C-A

952357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156325987-C-T

952391-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156325980-T-A

952421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 156325947-A-G

952421-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 156325947-A-T

952434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156325934-T-C

952455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156325913-T-C

952524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 156325844-C-T

952557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156325811-G-A

952557-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156325811-G-C

952675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156325708-G-A

952675-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156325708-G-T

http://identifiers.org/hco/1/GRCh38#952686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156325697-C-A

952686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156325697-C-T

http://identifiers.org/hco/1/GRCh38#952706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156325679-C-A

952706-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156325679-C-G

952713-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156325672-A-T

952722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156325663-A-G

952859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156325426-C-T

952907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156325367-G-A

952987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156325304-G-A

952987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156325304-G-T

953004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156325291-C-T

953067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156325244-A-G

http://identifiers.org/hco/1/GRCh38#953077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156325234-C-A

953077-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156325234-C-G

953077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156325234-C-T

953084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156325227-G-A

953084-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156325227-G-C

953084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156325227-G-T

953155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156325187-G-A

953155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156325187-G-T

953181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 156325162-G-A

953212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156325131-C-T

953224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156325119-C-T

953251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156325092-A-G

953254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156325089-G-A

953254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156325089-G-T

953260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156325083-T-C

953278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156325065-A-G

http://identifiers.org/hco/1/GRCh38#953344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156325011-C-A

953344-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156325011-C-G

http://identifiers.org/hco/1/GRCh38#953383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156324998-C-A

953417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156324986-G-A

953417-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156324986-G-C

953417-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156324986-G-T

953575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156324964-G-A

953575-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156324964-G-C

953577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156324962-C-T

http://identifiers.org/hco/1/GRCh38#953635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156324903-C-A

953635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156324903-C-T

953644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156324901-T-C

953666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156324890-G-A

953666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156324890-G-T

953667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156324889-G-A

953667-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156324889-G-C

953667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156324889-G-T

953693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156324862-G-A

953693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156324862-G-T

953713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156324842-A-G

953764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156324840-G-A

953764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156324840-G-T

953768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156324836-A-G

953768-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156324836-A-T

953773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156324831-G-A

953773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156324831-G-T

http://identifiers.org/hco/1/GRCh38#953788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156324816-C-A

953897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 156324707-G-A

953902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156324704-G-A

953941-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156324677-T-A

953941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156324677-T-C

954008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156324620-A-G

954011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156324617-G-A

954065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156324563-C-T

954088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 156324543-G-A

http://identifiers.org/hco/1/GRCh38#955977-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156323881-A-C

955977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156323881-A-G

956054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156323806-C-T

956065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156323795-G-A

956065-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156323795-G-C

956082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156323773-C-T

956106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156323746-G-A

956203-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156323649-G-C

956232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156323621-A-G

956253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156323600-G-A

956253-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156323600-G-C

956253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156323600-G-T

956258-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156323594-T-A

956258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156323594-T-C

956294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156323559-A-G

956295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156323558-G-A

956295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156323558-G-T

956448-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156323417-G-C

956476-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156323388-G-C

956476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156323388-G-T

956839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156322242-G-T

956853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156322226-C-T

http://identifiers.org/hco/1/GRCh38#956874-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156322203-C-A

956874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156322203-C-T

956878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156322199-C-T

956880-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156322197-T-A

956905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 156322172-G-A

956925-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156322152-G-C

956957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 156322117-C-T

956975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 156322099-T-C

956976-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156322098-C-G

956980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156322094-C-T

957011-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156322069-C-G

957011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 156322069-C-T

957018-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156322062-C-G

957018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156322062-C-T

957049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156322024-G-A

957061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156322012-G-A

http://identifiers.org/hco/1/GRCh38#957072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156321998-C-A

957072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156321998-C-T

957092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 156321979-C-T

http://identifiers.org/hco/1/GRCh38#957130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156321941-C-A

957130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156321941-C-T

957140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156321931-C-T

957154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156321917-G-A

957154-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156321917-G-C

957190-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156321881-T-A

957190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156321881-T-C

957208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156321863-T-C

957253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156321818-G-A

957256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156321815-G-A

957265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156321806-T-C

957266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156321805-T-C

957269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156321802-G-A

957269-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156321802-G-C

957281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 156321790-G-A

957281-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 156321790-G-C

958951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156320746-G-A

958957-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156320740-C-G

958957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156320740-C-T

http://identifiers.org/hco/1/GRCh38#958961-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156320736-A-C

958962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156320735-C-T

958966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156320731-G-A

958966-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156320731-G-C

958966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 156320731-G-T

http://identifiers.org/hco/1/GRCh38#958972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156320725-C-A

958972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156320725-C-T

958992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156320699-T-C

958999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 156320692-G-A

958999-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156320692-G-C

959002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156320689-G-A

959018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 156320673-G-A

959025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156320666-G-A

959034-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156320657-T-G

959046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156320645-G-A

959048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 156320643-T-C

959064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156320627-G-A

959064-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156320627-G-C

959064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156320627-G-T

959084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 156320607-G-A

959084-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 156320607-G-C

959087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 156320604-G-A

959087-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 156320604-G-C

959087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 156320604-G-T

959088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 156320603-G-A

959088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 156320603-G-T

959093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156320598-G-A

959093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156320598-G-T

959101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156320585-C-T

959161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156320556-T-C

959161-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156320556-T-G

http://identifiers.org/hco/1/GRCh38#959175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156320542-C-A

959175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156320542-C-T

http://identifiers.org/hco/1/GRCh38#959177-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156320540-A-C

959178-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156320539-C-G

959229-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 156320511-C-G

959229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 156320511-C-T

959240-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: non_coding_transcript_exon_variant, start_lost
orthologous variants: 156320500-T-A

959240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: non_coding_transcript_exon_variant, start_lost
orthologous variants: 156320500-T-C

959240-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: non_coding_transcript_exon_variant, start_lost
orthologous variants: 156320500-T-G

959245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 156320496-C-T

http://identifiers.org/hco/1/GRCh38#959248-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156320493-A-C

959248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 156320493-A-G

959277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: non coding transcript exon variant
orthologous variants: 156320464-C-T

http://identifiers.org/hco/1/GRCh38#959292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156320449-C-A

959292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: non coding transcript exon variant
orthologous variants: 156320449-C-T

959304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: non coding transcript exon variant
orthologous variants: 156320437-G-A

959304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24517
most severe consequence: non coding transcript exon variant
orthologous variants: 156320437-G-T