53001450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78079258-C-T

53001455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78079253-T-C

53001458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78079250-T-C

53001458-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78079250-T-G

53001467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78079246-G-A

53001534-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78079198-A-T

53001546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78079186-G-T

53001734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78079006-C-T

53001939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78078808-G-T

53002062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78078678-A-G

53002062-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78078678-A-T

53002089-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78078656-A-T

53002300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78078428-A-G

http://identifiers.org/hco/6/GRCh38#53002320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78078279-C-A

53002963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78077679-T-C

53003153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78077509-T-C

53003176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78077486-A-G

http://identifiers.org/hco/6/GRCh38#53003207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78077455-C-A

53003398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78077300-C-T

53003405-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78077293-A-T

53003431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78077273-C-T

53003768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78077231-G-T

53003788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78077213-A-G

http://identifiers.org/hco/6/GRCh38#53003869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78077129-C-A

http://identifiers.org/hco/6/GRCh38#53003924-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78077073-A-C

53003927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78077070-G-A

53003969-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78077028-T-G

http://identifiers.org/hco/6/GRCh38#53004003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78076994-C-A

53004184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78076800-A-G

53004639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78075490-G-T

53004652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78075477-A-G

http://identifiers.org/hco/6/GRCh38#53004920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78075227-C-A

53004920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78075227-C-T

53005011-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78075138-T-A

53005011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78075138-T-C

53005011-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78075138-T-G

53005219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 78074964-G-A

53005219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 78074964-G-T

53005231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 78074952-G-T

http://identifiers.org/hco/6/GRCh38#53005867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78074685-C-A

http://identifiers.org/hco/6/GRCh38#53006019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78074551-C-A

53006244-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78074379-G-C

53006244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78074379-G-T

53006274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78074349-T-C

53006291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78074336-T-C

53006302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78074325-A-G

53006389-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 78074238-G-C

53006475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78074151-C-T

53006484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78074144-A-G

53006509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78074122-G-A

53006509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78074122-G-T

53006560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78074089-A-G

53006912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78073787-C-T

53006927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78073754-T-C

53007183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78073442-G-A

53007373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78073294-G-T

53007413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78073259-T-C

53007413-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78073259-T-G

53007414-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78073258-A-T

53009342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78072030-T-C

53009371-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78072004-T-G

53009588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78071790-T-C

http://identifiers.org/hco/6/GRCh38#53009606-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78070176-A-C

http://identifiers.org/hco/6/GRCh38#53009617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78070166-C-A

53009617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78070166-C-T

53009672-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78070119-T-A

http://identifiers.org/hco/6/GRCh38#53009791-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78069942-A-C

53009791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78069942-A-G

53009993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78069742-A-G

53010455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78069207-C-T

53010849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78068740-G-A

53010871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78068716-G-A

53010884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78068707-G-A

53010940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78068641-C-T

53011250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78068299-G-A

53011552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78068200-T-C

53011623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78068178-C-T

53011720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78068138-A-G

http://identifiers.org/hco/6/GRCh38#53011735-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78068123-A-C

53011881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 78067979-A-G

http://identifiers.org/hco/6/GRCh38#53012280-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#78067595-A-C

53012283-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78067592-C-G

53013043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78066532-A-G

53013100-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78066467-T-A

53013555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78065341-A-G

53013555-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78065341-A-T

53013629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78065272-C-T

53013646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 78065247-A-G

53013691-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 78065203-G-C

53013702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 78065192-G-A

53013702-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 78065192-G-C

53013724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 78065170-G-A

53013756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 78065138-G-A

53014007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78064896-G-A

http://identifiers.org/hco/6/GRCh38#53014898-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78064056-A-C

53014899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78064055-T-C

http://identifiers.org/hco/6/GRCh38#53014935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78064016-C-A

53014935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78064016-C-T

53015425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78063622-C-T

53015443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78063604-G-A

53015563-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78063487-G-C

http://identifiers.org/hco/6/GRCh38#53015639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78063420-C-A

53015773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78063288-T-C

http://identifiers.org/hco/6/GRCh38#53015929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78062969-C-A

53015929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78062969-C-T

53016276-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78062607-C-G

http://identifiers.org/hco/6/GRCh38#53016285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78062598-C-A

53016300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78062582-T-C

http://identifiers.org/hco/6/GRCh38#53016325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78062559-C-A

53016325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78062559-C-T

53016441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78062469-G-A

53016466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78062445-G-A

53016466-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78062445-G-C

53016471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78062440-G-T

53016687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78062202-T-C

53016765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78062135-T-C

53016827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78062074-C-T

53017761-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78061463-T-A

53017761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78061463-T-C

http://identifiers.org/hco/6/GRCh38#53017767-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78061457-A-C

53017767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78061457-A-G

53017893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78061339-G-A

53018207-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78061119-A-T

53018232-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78061097-G-C

53018232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78061097-G-T

53018305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78061040-A-G

53018305-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78061040-A-T

53019023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78058319-A-G

http://identifiers.org/hco/6/GRCh38#53019117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78058236-C-A

53019173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78057998-T-C

53019183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78057988-T-C

53019192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78057976-T-C

53019199-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78057969-A-T

53019209-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78057959-G-C

http://identifiers.org/hco/6/GRCh38#53019405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78057769-C-A

53019405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78057769-C-T

53019423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78057751-T-C

53019503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78057723-A-G

53019507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78057719-T-C

53019507-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78057719-T-G

53020293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78057080-A-G

53020325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78057046-C-T

53021602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78056226-T-C

53022672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78056143-T-C

53022809-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78056026-T-A

53022809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78056026-T-C

53022809-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78056026-T-G

53023471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78055686-G-A

53023570-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78055594-G-C

53023704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78055464-T-C

53023781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78055385-C-T

53023842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78055329-G-A

53023842-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78055329-G-C

53023867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78055304-T-C

53023962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78055213-A-G

53023973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78055202-G-A

53023989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78055186-C-T

53024148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78055019-T-C

53024360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78054808-T-C

53024387-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78054781-A-T

53024517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78054646-G-A

53024545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78054625-G-T

53025309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78054229-C-T

53025343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78054196-A-G

53025493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78054065-C-T

53026487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78053734-T-C

53026512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78053709-T-C

53026533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78053688-T-C

53027146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78053060-T-C

53027193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78053003-T-C

53027315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78052889-T-C

http://identifiers.org/hco/6/GRCh38#53027334-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78052871-A-C

53027339-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78052866-G-C

53027612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78052589-A-G

53027612-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78052589-A-T

53028460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78052193-T-C

53028520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78052134-C-T

53028824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78051842-T-C

53028891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78051758-T-C

53029368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78051367-G-A

http://identifiers.org/hco/6/GRCh38#53029388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78051347-C-A

http://identifiers.org/hco/6/GRCh38#53029435-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78051301-A-C

53029546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78051204-T-C

53029813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78051051-A-G

53029948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78050949-G-A

53029948-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78050949-G-C

53030006-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78050900-T-A

53030178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78050731-C-T

53030231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78050687-G-A

53030250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78050668-T-C

53030335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78050581-C-T

53030655-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78048945-T-G

53030748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78048852-C-T

53030749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78048851-A-G

53030976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78048639-G-T

53030989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78048626-T-C

53030990-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78048625-T-G

53031164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78048454-A-G

http://identifiers.org/hco/6/GRCh38#53031277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78048275-C-A

53032240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78047778-C-T

http://identifiers.org/hco/6/GRCh38#53032323-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78047693-A-C

http://identifiers.org/hco/6/GRCh38#53032524-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78047386-A-C

53032593-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 78047317-T-A

53032593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 78047317-T-C

53032694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78047225-A-G

53032739-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78047180-T-A

53032747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78047172-A-G

http://identifiers.org/hco/6/GRCh38#53032772-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78047150-A-C

53032775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78047147-T-C

http://identifiers.org/hco/6/GRCh38#53032779-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78047141-A-C

53032779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78047141-A-G

53032862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78047048-G-A

53032873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78047037-G-A

53032875-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78047035-A-T

53032894-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78047016-T-A

53032981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78046904-G-A

53032987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78046898-G-A

53032999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78046886-A-G

53033111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78046680-G-A

53033172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78046609-C-T

53033267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78046525-A-G

http://identifiers.org/hco/6/GRCh38#53033550-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78046265-A-C

53033583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78046237-C-T

53033587-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78046233-T-G

53033742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78045895-C-T

53033935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78045740-T-C

53034105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78045599-C-T

53034110-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78045594-T-A

53034120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78045584-G-A

53034145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78045572-C-T

53034306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78045426-C-T

53034439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78045329-T-C

53034577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78045198-G-A

53036978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78044007-A-G

53037376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78043638-G-A

http://identifiers.org/hco/6/GRCh38#53037587-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78043283-A-C

53037689-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78043179-A-T

http://identifiers.org/hco/6/GRCh38#53037782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78043095-C-A

53037807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78043063-T-C

53037850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78043020-A-G

53040388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78039487-C-T

53040399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78039476-A-G

53040415-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78039458-G-C

http://identifiers.org/hco/6/GRCh38#53041060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78038954-C-A

53041060-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78038954-C-G

53041205-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 78038782-C-G

53041205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 78038782-C-T

http://identifiers.org/hco/6/GRCh38#53041390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78038593-C-A

53041424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78038559-A-G

53041532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78038407-T-C

53041554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78038385-T-C

53041554-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78038385-T-G

53042336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78038199-C-T

53042486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78038052-C-T

53042645-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78037879-A-T

53042922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78037662-G-A

53043070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78037629-C-T

53043368-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78037555-G-C

53043393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78037531-G-A

53043557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78037397-C-T

53043769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78037225-G-A

53043769-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78037225-G-C

53043943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78037067-T-C

53046081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78034272-T-C

53047009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78033391-A-G

53048025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78032578-C-T

53048217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78032412-A-G

53048339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78032317-G-A

53048587-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78032086-T-A

53049081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78031603-T-C

53049442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78030679-G-A

53054664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78029613-T-C

53054789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78029505-A-G

53054795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78029499-G-T

53054832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78029462-C-T

53054892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78029418-G-A

53054892-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78029418-G-C

53055305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78029192-T-C

53055384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78029119-T-C

53055475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78029029-G-A

53055549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78028955-C-T

53055558-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78028951-G-C

53056225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78028539-G-A

53056417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78028373-A-G

53056425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78028365-A-G

http://identifiers.org/hco/6/GRCh38#53056525-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78028303-A-C

53057429-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78026871-T-G

53057577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78026834-T-C

53057577-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78026834-T-G

53057612-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78026805-T-A

53057612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78026805-T-C

53057815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78025932-T-C

53057878-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78025881-C-G

53057878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78025881-C-T

53058150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78025701-T-C

53058287-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78025576-T-G

53058290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78025573-G-A

53058332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78025535-A-G

http://identifiers.org/hco/6/GRCh38#53058454-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78025270-A-C

53058527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78025197-C-T

53058565-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78025163-C-G

53058565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78025163-C-T

53058588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78025144-A-G

53058761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78024154-C-T

53058795-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78023607-A-T

53059134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78023284-C-T

53059150-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78023268-A-T

53059153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78023265-C-T

53059159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78023259-T-C

53059634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78022807-C-T

53059731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78022549-A-G

53059744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78022536-C-T

53060023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78022279-T-C

53060056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78022265-T-C

53060170-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78022137-G-C

53060377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78021940-T-C

53060490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78021795-T-C

53060837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78021461-G-A

53061017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78021302-T-C

53061337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78020971-G-A

53061466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78020836-A-G

53061558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78020774-G-A

53061558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21219
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78020774-G-T