92947541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 5 prime UTR variant
orthologous variants: 49473620-G-A

92947541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 5 prime UTR variant
orthologous variants: 49473620-G-T

http://identifiers.org/hco/9/GRCh38#92947600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49473550-C-A

92947667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 5 prime UTR variant
orthologous variants: 49473479-G-A

92947667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 5 prime UTR variant
orthologous variants: 49473479-G-T

http://identifiers.org/hco/9/GRCh38#92947680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49473466-C-A

92947680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 5 prime UTR variant
orthologous variants: 49473466-C-T

92947835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: intron variant
orthologous variants: 49473352-C-T

92947992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: intron variant
orthologous variants: 49473226-G-T

92948245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: intron variant
orthologous variants: 49472993-A-G

92948932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: intron variant
orthologous variants: 49471851-G-A

http://identifiers.org/hco/9/GRCh38#92949071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49471729-C-A

92952745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: intron variant
orthologous variants: 49470809-C-T

92952782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: intron variant
orthologous variants: 49470775-C-T

92952834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: intron variant
orthologous variants: 49470727-C-T

92952957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: intron variant
orthologous variants: 49470614-T-C

92953100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: intron variant
orthologous variants: 49470468-G-A

92953802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: intron variant
orthologous variants: 49469764-A-G

92954118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: intron variant
orthologous variants: 49469436-C-T

92954163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: intron variant
orthologous variants: 49469406-A-G

92954236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: intron_variant, undefined
orthologous variants: 49469345-G-A

92962633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: intron variant
orthologous variants: 49463944-A-G

http://identifiers.org/hco/9/GRCh38#92964077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49462926-C-A

http://identifiers.org/hco/9/GRCh38#92964123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49462873-C-A

92964123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49462873-C-T

92964293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49462714-G-T

92964342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49462665-T-C

92964365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: intron variant
orthologous variants: 49462642-T-C

92964438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: intron variant
orthologous variants: 49462560-G-T

92964446-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: intron variant
orthologous variants: 49462545-G-T

92964646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: intron variant
orthologous variants: 49462374-G-A

92964646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: intron variant
orthologous variants: 49462374-G-T

92964655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: intron variant
orthologous variants: 49462355-T-C

http://identifiers.org/hco/9/GRCh38#92964883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49462200-C-A

92964883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: intron variant
orthologous variants: 49462200-C-T

http://identifiers.org/hco/9/GRCh38#92964939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49462147-C-A

92964972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: intron variant
orthologous variants: 49462116-G-A

92965050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: intron variant
orthologous variants: 49462035-A-G

92965505-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: intron variant
orthologous variants: 49461090-A-T

92965787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: intron variant
orthologous variants: 49460829-T-C

http://identifiers.org/hco/9/GRCh38#92965998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49460568-C-A

92974180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: intron variant
orthologous variants: 49452777-G-T

92974462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: intron variant
orthologous variants: 49452292-G-A

92974462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: intron variant
orthologous variants: 49452292-G-T

92974572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49452187-T-C

http://identifiers.org/hco/9/GRCh38#92974574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49452185-C-A

92974574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49452185-C-T

http://identifiers.org/hco/9/GRCh38#92974694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49452110-C-A

92974696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49452108-T-C

92974728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49452076-G-T

92974829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49451963-G-A

92974829-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49451963-G-C

92974829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49451963-G-T

92974987-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49451766-C-G

http://identifiers.org/hco/9/GRCh38#92975072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49451688-C-A

92975112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49451653-G-T

92975182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49451581-T-C

http://identifiers.org/hco/9/GRCh38#92975443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49451352-C-A

92975455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49451340-T-C

http://identifiers.org/hco/9/GRCh38#92975469-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49451326-A-C

92975469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49451326-A-G

92975481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49451317-T-C

92975482-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49451316-T-A

http://identifiers.org/hco/9/GRCh38#92975500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49451298-C-A

http://identifiers.org/hco/9/GRCh38#92975528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49451270-C-A

92975529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49451269-T-C

92976109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49450365-G-A

92976109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49450365-G-T

92976118-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49450356-T-A

92976118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49450356-T-C

92976118-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49450356-T-G

http://identifiers.org/hco/9/GRCh38#92976119-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49450355-A-C

92976119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49450355-A-G

92976119-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49450355-A-T

92976140-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49450333-G-C

92976140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49450333-G-T

http://identifiers.org/hco/9/GRCh38#92976199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49450304-C-A

92976199-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49450304-C-G

92976199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49450304-C-T

92976209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 49450294-A-G

http://identifiers.org/hco/9/GRCh38#92976236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49450266-C-A

92976236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 49450266-C-T

92976273-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49450229-G-C

92976273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49450229-G-T

92976383-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49450116-T-A

92976383-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49450116-T-G

92976395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49450104-G-A

92976395-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49450104-G-C

92976446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49450068-G-A

92976446-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49450068-G-C

http://identifiers.org/hco/9/GRCh38#92976676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49449838-C-A

92976676-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 49449838-C-G

92976676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 49449838-C-T

http://identifiers.org/hco/9/GRCh38#92976700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49449814-C-A

92976769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49449755-G-A

92976812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49449712-G-T

92976813-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49449711-T-A

93002778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49443230-A-G

http://identifiers.org/hco/9/GRCh38#93002786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49443222-C-A

http://identifiers.org/hco/9/GRCh38#93002792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49443216-C-A

http://identifiers.org/hco/9/GRCh38#93002805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49443206-C-A

93002805-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49443206-C-G

http://identifiers.org/hco/9/GRCh38#93002834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49443185-C-A

93002835-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49443184-C-G

93002863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49443172-G-A

93002863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49443172-G-T

93002909-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49443143-T-G

93003044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49442984-G-A

93003046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49442982-A-G

93003046-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49442982-A-T

93003060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49442968-G-A

93003062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49442966-T-C

93003104-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49442926-T-A

93003104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49442926-T-C

93003118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49442912-G-A

93003118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49442912-G-T

93003620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 49442375-G-A

93003863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 49442171-A-G

93003863-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 49442171-A-T

http://identifiers.org/hco/9/GRCh38#93003870-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#49442164-A-C

93003871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 49442163-A-G

93004016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 49440881-C-T

93004082-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 49440815-C-G

93004082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 49440815-C-T

http://identifiers.org/hco/9/GRCh38#93004152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#49440745-C-A

93004152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 49440745-C-T

http://identifiers.org/hco/9/GRCh38#93004195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#49440714-C-A

93004270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49440638-T-C

93004294-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 49440617-T-A

93004396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49440581-C-T

93004434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49440546-A-G

93004449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49440531-C-T

93005472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49440242-G-T

93005931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49439375-C-T

93006091-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 49439257-T-G

http://identifiers.org/hco/9/GRCh38#93006148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49439200-C-A

93006148-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 49439200-C-G

93008174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49437420-T-C

93008232-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49437370-C-G

93008315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49437289-G-A

93008322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49437282-C-T

93008341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49437268-C-T

93009487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49436088-G-T

http://identifiers.org/hco/9/GRCh38#93009615-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49435977-A-C

93009921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49435684-A-G

93009938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49435661-C-T

93010158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49435503-T-C

93010167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49435494-C-T

93010212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49435464-C-T

93010237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49435438-T-C

93010352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49435323-C-T

93010395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49435280-G-A

93010761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49435145-T-C

93010768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49435138-C-T

93010832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49435101-G-A

93010832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49435101-G-T

http://identifiers.org/hco/9/GRCh38#93010833-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49435100-A-C

http://identifiers.org/hco/9/GRCh38#93011092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49434877-C-A

93011092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49434877-C-T

93011109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49434860-G-T

93011110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49434859-G-A

93011110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49434859-G-T

http://identifiers.org/hco/9/GRCh38#93011111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49434858-C-A

93011111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49434858-C-T

http://identifiers.org/hco/9/GRCh38#93011169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49434795-C-A

93011169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49434795-C-T

93011313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49434652-G-T

93011368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49434599-G-A

93011368-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49434599-G-C

93011368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49434599-G-T

http://identifiers.org/hco/9/GRCh38#93012870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49434541-C-A

http://identifiers.org/hco/9/GRCh38#93013218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49434302-C-A

93013262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49434261-C-T

93013282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49434241-C-T

93013665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49433870-A-G

http://identifiers.org/hco/9/GRCh38#93013783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49433749-C-A

93013876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49433648-G-T

93013969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49433555-G-A

93014045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49433490-T-C

93014476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49433118-C-T

http://identifiers.org/hco/9/GRCh38#93015703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49432104-C-A

93015703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49432104-C-T

93015722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49432095-C-T

93015803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49432014-G-A

93015857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49431964-G-A

93015858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49431963-T-C

93016020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49431857-G-A

93016151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49431721-T-C

93016184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49431689-T-C

93016229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49431651-G-A

93017669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49431539-G-T

93017712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49431493-C-T

93017981-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49431282-A-T

93018050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49431215-G-A

93018056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49431183-A-G

http://identifiers.org/hco/9/GRCh38#93018057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49431182-C-A

93018057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49431182-C-T

93018087-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49431142-T-A

93018258-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49430960-T-A

93018258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49430960-T-C

93019780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49429164-T-C

93019891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49429037-A-G

93020005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49428762-G-A

93020005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49428762-G-T

http://identifiers.org/hco/9/GRCh38#93020045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49428722-C-A

93020170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49428604-T-C

http://identifiers.org/hco/9/GRCh38#93021639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49427862-C-A

93021695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49427816-C-T

93021705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49427803-A-G

93021814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49427656-C-T

93021851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49427621-G-T

93021925-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49427572-G-C

93021933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49427564-C-T

93021935-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49427562-G-C

93022105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49427427-C-T

93022137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49427408-C-T

93022145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49427400-G-A

93022153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49427392-C-T

http://identifiers.org/hco/9/GRCh38#93022196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49427367-C-A

93022196-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49427367-C-G

93022196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49427367-C-T

93022220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49427347-G-A

93022220-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49427347-G-C

93022220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49427347-G-T

93022245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49427326-G-A

93022245-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49427326-G-C

93022245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49427326-G-T

93022325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, undefined
orthologous variants: 49427248-A-G

93022384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 49427189-G-A

http://identifiers.org/hco/9/GRCh38#93022397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49427176-C-A

93022397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 49427176-C-T

93022406-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49427167-C-G

93022406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49427167-C-T

93022422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49427151-T-C

93022502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49427111-G-A

93022502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49427111-G-T

93022517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49427096-G-A

93022545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49427069-G-A

93023389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49425692-G-A

93023539-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49425540-C-G

93023539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49425540-C-T

93023552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49425527-T-C

93023606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49425479-C-T

93024342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49425134-C-T

93024520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49425026-C-T

93024926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49424716-C-T

93024979-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49424670-C-G

93024979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49424670-C-T

93024980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49424669-G-A

93025013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49424636-C-T

93025126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49424516-G-A

http://identifiers.org/hco/9/GRCh38#93026201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49423387-C-A

93026201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49423387-C-T

93026202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49423386-G-A

93029342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49422350-C-T

93029464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49422208-C-T

93029563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49422115-A-G

93029610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49422066-T-C

http://identifiers.org/hco/9/GRCh38#93029617-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49422059-A-C

93029617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49422059-A-G

93029750-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49421969-T-A

93029750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49421969-T-C

http://identifiers.org/hco/9/GRCh38#93029757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49421962-C-A

93029757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49421962-C-T

93029772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49421948-C-T

http://identifiers.org/hco/9/GRCh38#93029780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49421940-C-A

93029800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49421918-G-A

93029800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49421918-G-T

http://identifiers.org/hco/9/GRCh38#93029812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49421906-C-A

93029812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49421906-C-T

93029850-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49421853-T-A

93029850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49421853-T-C

93029874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 49421829-C-T

http://identifiers.org/hco/9/GRCh38#93029887-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49421816-A-C

93029889-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49421814-C-G

http://identifiers.org/hco/9/GRCh38#93030048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49421645-C-A

93030048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49421645-C-T

93032444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49420465-G-T

http://identifiers.org/hco/9/GRCh38#93032451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49420458-C-A

93032451-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49420458-C-G

93032451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49420458-C-T

93032463-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49420447-T-A

93032464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49420446-G-T

http://identifiers.org/hco/9/GRCh38#93032527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49420390-C-A

93032661-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49420262-G-T

93032695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49420255-T-C

93032964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 49420058-G-T

93032977-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 49420049-C-G

93032983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 49420043-G-A

93032983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 49420043-G-T

93032989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 49420037-G-T

http://identifiers.org/hco/9/GRCh38#93032994-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49420032-A-C

93032994-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49420032-A-T

93033054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49419969-G-A

93033054-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49419969-G-C

93033069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49419951-G-A

93033069-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49419951-G-C

93033069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49419951-G-T

93033071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49419948-G-A

93033071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49419948-G-T

93033076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49419943-G-A

93033076-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49419943-G-C

93033079-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49419940-A-T

93033095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49419930-A-G

93033102-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49419923-T-A

http://identifiers.org/hco/9/GRCh38#93033108-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49419917-C-A

93033108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49419917-C-T

http://identifiers.org/hco/9/GRCh38#93033169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49419862-C-A

http://identifiers.org/hco/9/GRCh38#93033227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49419827-C-A

93033227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49419827-C-T

93033258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49419788-C-T

http://identifiers.org/hco/9/GRCh38#93033455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49419562-C-A

93033455-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49419562-C-G

93033455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49419562-C-T

93033564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49419383-G-T

93033568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49419379-C-T

93033658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49419326-A-G

93033658-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49419326-A-T

93033671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49419313-T-C

93033697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49419269-A-G

93033795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49419171-G-A

93033795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49419171-G-T

93033796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49419170-T-C

93033804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49419162-G-A

93033804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49419162-G-T

93033876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49419116-T-C

http://identifiers.org/hco/9/GRCh38#93033940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49419048-C-A

http://identifiers.org/hco/9/GRCh38#93033960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49419028-C-A

93033960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49419028-C-T

93033979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49419009-C-T

93034124-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49418879-C-G

http://identifiers.org/hco/9/GRCh38#93034136-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49418862-C-A

93034139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49418852-T-C

93034139-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49418852-T-G

93034198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49418780-T-C

http://identifiers.org/hco/9/GRCh38#93034211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49418753-C-A

93034222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49418740-T-C

93034222-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49418740-T-G

http://identifiers.org/hco/9/GRCh38#93034226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49418736-C-A

93034226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49418736-C-T

93034231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49418731-A-G

93034276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49418613-G-A

93034276-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49418613-G-C

93034276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49418613-G-T

93034309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49418528-T-C

93034309-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49418528-T-G

93034320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49418507-G-A

93034320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49418507-G-T

http://identifiers.org/hco/9/GRCh38#93034332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49418462-C-A

93034332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49418462-C-T

93034392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49418406-A-G

93034393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49418405-G-A

93034393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49418405-G-T

93034427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49418371-G-T

http://identifiers.org/hco/9/GRCh38#93034432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49418366-C-A

http://identifiers.org/hco/9/GRCh38#93034445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49418350-C-A

93034458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49418337-C-T

93034474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49418321-G-A

93034474-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49418321-G-C

http://identifiers.org/hco/9/GRCh38#93034495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49418299-C-A

93034495-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49418299-C-G

93034507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49418287-A-G

93034561-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 49418233-C-G

93034561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 49418233-C-T

93034689-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 49418105-T-A

93034689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 49418105-T-C

http://identifiers.org/hco/9/GRCh38#93034694-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49418100-A-C

93034694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49418100-A-G

93034703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49418091-G-A

93034703-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49418091-G-C

93034703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49418091-G-T

http://identifiers.org/hco/9/GRCh38#93034707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49418087-C-A

93034707-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49418087-C-G

93034707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49418087-C-T

93034711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49418083-G-T

93034714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49418080-C-T

93034725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49418049-A-G

http://identifiers.org/hco/9/GRCh38#93034754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49418020-C-A

93034754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49418020-C-T

http://identifiers.org/hco/9/GRCh38#93034774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49418000-C-A

93034777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49417997-C-T

93034792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49417987-T-C

93034792-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49417987-T-G

http://identifiers.org/hco/9/GRCh38#93034811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49417969-C-A

93034811-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49417969-C-G

93034811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49417969-C-T

93034819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49417961-G-A

93034819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49417961-G-T

93035182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49417607-A-G

93035293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49417538-G-A

93035293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49417538-G-T

93035401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 49417446-G-A

93035410-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 49417437-G-C

http://identifiers.org/hco/9/GRCh38#93035461-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49417386-A-C

93035461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 49417386-A-G

http://identifiers.org/hco/9/GRCh38#93035485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49417362-C-A

93035485-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 49417362-C-G

93035514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 49417333-T-C

93035517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 49417330-C-T

93035546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 49417301-G-A

93035546-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 49417301-G-C

http://identifiers.org/hco/9/GRCh38#93035591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49417256-C-A

93035591-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 49417256-C-G

http://identifiers.org/hco/9/GRCh38#93035603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49417244-C-A

http://identifiers.org/hco/9/GRCh38#93035618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49417229-C-A

93035618-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 49417229-C-G

http://identifiers.org/hco/9/GRCh38#93035659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49417189-C-A

93035659-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 49417189-C-G

93035659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 49417189-C-T

93035687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 49417153-G-A

93035687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 49417153-G-T

93035758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 49417125-A-G

http://identifiers.org/hco/9/GRCh38#93035760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49417123-C-A

93035760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 49417123-C-T

93035809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 49417061-A-G

93035809-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 49417061-A-T

http://identifiers.org/hco/9/GRCh38#93035827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49417044-C-A

93035834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 49417037-G-A

93035834-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 49417037-G-T

http://identifiers.org/hco/9/GRCh38#93035845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49417022-C-A

93035845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 49417022-C-T

93035911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 49416966-T-C

93035960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 49416890-C-T

93036023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 49416827-T-C

93036023-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 49416827-T-G

http://identifiers.org/hco/9/GRCh38#93036106-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49416728-A-C

93036153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 49416681-C-T

93036172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 49416662-G-T

93036175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 49416658-G-A

93036175-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 49416658-G-C

93036175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 49416658-G-T

93036201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 49416634-C-T

93036230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 49416605-A-G