37433072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 29879464-C-T

37433171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 29879545-G-A

http://identifiers.org/hco/6/GRCh38#37433238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#29879609-C-A

37433238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 29879609-C-T

37433271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 29879633-T-C

http://identifiers.org/hco/6/GRCh38#37433350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#29879718-C-A

37433350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 29879718-C-T

37433454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29879821-G-A

37433454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29879821-G-T

37433482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29879842-T-C

37433482-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29879842-T-G

37433489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29879850-G-A

37433489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29879850-G-T

http://identifiers.org/hco/6/GRCh38#37433501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29879862-C-A

37433501-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29879862-C-G

37433501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29879862-C-T

37433590-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29879932-C-G

37433590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29879932-C-T

37434122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29880353-A-G

37434185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29880421-C-T

37434761-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29880994-C-G

37434765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29880998-C-T

37434769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29881004-C-T

37435506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29882027-G-T

http://identifiers.org/hco/6/GRCh38#37435537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29882058-C-A

37435684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 29882202-A-G

37435851-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29882364-C-G

37436457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29883446-G-A

37436457-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29883446-G-C

37436496-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29883472-T-G

37436650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29883630-A-G

http://identifiers.org/hco/6/GRCh38#37436902-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29883893-A-C

37436915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29883906-C-T

37436953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29883944-A-G

37436992-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29883983-T-G

37437003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29883994-T-C

37438731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29885367-C-T

37439007-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29885586-A-T

37439165-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29885728-G-C

37439311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29885876-G-A

37439475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29886032-G-A

37439984-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29886367-T-G

37440340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29886714-C-T

http://identifiers.org/hco/6/GRCh38#37440550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29886906-C-A

37440837-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29887163-C-G

37440837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29887163-C-T

37440912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29887236-A-G

37441153-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29887455-A-T

37442385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29888757-G-A

37443865-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29892990-T-G

http://identifiers.org/hco/6/GRCh38#37443923-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29893039-A-C

37443977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29893091-C-T

37444332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29893845-T-C

http://identifiers.org/hco/6/GRCh38#37445158-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29894320-A-C

37445270-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29894415-G-C

37446102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29894935-G-A

http://identifiers.org/hco/6/GRCh38#37446506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29895321-C-A

37446506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29895321-C-T

37446939-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29896068-G-C

37447173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29896357-A-G

37447279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29896455-G-A

37447555-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29896716-C-G

37448533-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29897116-C-G

37449935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29897660-G-A

37450012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29897736-A-G

37450274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: synonymous variant
orthologous variants: 29897987-A-G

37450691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29898332-A-G

37450761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29898400-T-C

37450802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29898432-T-C

37450802-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29898432-T-G

37450819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29898444-C-T

37451621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29899391-C-T

37451766-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29899523-T-A

37451920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29899671-G-T

37451959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29899716-G-A

37451959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29899716-G-T

37452141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29899897-G-A

37452213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29899964-C-T

37452349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29900065-C-T

37452732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29900597-A-G

37452732-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29900597-A-T

37453211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29901056-T-C

37453213-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29901069-G-C

37453353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29901191-G-T

http://identifiers.org/hco/6/GRCh38#37453429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29901265-C-A

37453429-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29901265-C-G

37453429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29901265-C-T

37453932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29901359-G-A

37453944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29901371-C-T

37454235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29901658-C-T

37454553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29901975-T-C

37454587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29902009-A-G

37454672-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29902091-A-T

37454846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29902261-C-T

37456726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29903558-T-C

37456959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29903713-A-G

37457215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29903856-G-A

37457215-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29903856-G-C

37457215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29903856-G-T

37457437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29904022-G-A

37457437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29904022-G-T

37457559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29904123-T-C

37457827-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29904379-T-G

37457881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29904430-A-G

37458463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29904671-A-G

37458566-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29904781-G-C

37458566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29904781-G-T

37458850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29905065-A-G

37458851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29905066-G-A

37458920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29905129-T-C

37458942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29905153-T-C

37458966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29905189-A-G

37459507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29905961-T-C

37459712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29906152-T-C

37459786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29906319-G-T

http://identifiers.org/hco/6/GRCh38#37459795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29906328-C-A

37459795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29906328-C-T

37459846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29906379-T-C

37459856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29906389-G-T

37460549-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29907427-A-T

http://identifiers.org/hco/6/GRCh38#37460956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29907779-C-A

37460956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29907779-C-T

http://identifiers.org/hco/6/GRCh38#37461430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29908772-C-A

37461507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29908837-T-C

37461653-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 29908973-T-A

37461653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 29908973-T-C

37461657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29908977-T-C

http://identifiers.org/hco/6/GRCh38#37461661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29908981-C-A

37461661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29908981-C-T

http://identifiers.org/hco/6/GRCh38#37461708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29909025-C-A

37461708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29909025-C-T

37461717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29909033-G-A

37461717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29909033-G-T

37461811-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29909146-G-C

37461820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29909155-A-G

37462284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29909568-C-T

37462489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29909747-G-T

37462591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29909823-A-G

37462713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29910109-G-T

37463123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29910464-A-G

37463208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29910489-C-T

37463226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29910506-G-A

37463234-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29910514-C-G

37470911-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29913159-T-A

37470911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29913159-T-C

37470915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29913163-T-C

http://identifiers.org/hco/6/GRCh38#37470933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29913171-C-A

37471783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29913739-G-A

37471783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29913739-G-T

http://identifiers.org/hco/6/GRCh38#37472032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29913900-C-A

37472032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29913900-C-T

37472049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29913910-G-A

37472049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29913910-G-T

37472164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29914002-T-C

37472479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: synonymous variant
orthologous variants: 29914460-C-T

37472678-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29914632-C-G

37473052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29915721-G-A

37473275-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29915904-C-G

http://identifiers.org/hco/6/GRCh38#37473316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29915945-C-A

37473675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29916269-G-A

http://identifiers.org/hco/6/GRCh38#37473676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29916270-C-A

37473676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29916270-C-T

37474081-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29916637-C-G

37474155-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29916685-T-G

37474219-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29916735-T-G

37474274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29916759-C-T

37474698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29917095-G-A

37474698-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29917095-G-C

37474698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29917095-G-T

37474711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29917108-G-T

37474861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29917200-A-G

37474864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29917203-C-T

http://identifiers.org/hco/6/GRCh38#37475219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29917506-C-A

37475219-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29917506-C-G

37475254-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29917550-T-G

http://identifiers.org/hco/6/GRCh38#37475288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29917583-C-A

37475288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29917583-C-T

37475296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29917591-G-A

http://identifiers.org/hco/6/GRCh38#37475425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29917715-C-A

http://identifiers.org/hco/6/GRCh38#37475548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29917751-C-A

http://identifiers.org/hco/6/GRCh38#37475554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29917757-C-A

37475554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 29917757-C-T

37475696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 29917867-G-A

37475696-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 29917867-G-C

37475696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 29917867-G-T

37476809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29918572-G-A

37477267-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29918921-G-C

37477628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 29919244-G-A

37477704-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29919307-T-A

37477704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29919307-T-C

http://identifiers.org/hco/6/GRCh38#37477723-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29919326-A-C

37477723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29919326-A-G

37477723-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29919326-A-T

37477844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29919433-G-A

37478279-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29919794-T-A

37478279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29919794-T-C

37478279-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29919794-T-G

37478317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29919840-T-C

37478321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29919844-G-A

37478321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29919844-G-T

http://identifiers.org/hco/6/GRCh38#37478363-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29919888-C-A

37478363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29919888-C-T

37478424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 29919960-C-T

37478430-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 29919966-G-C

37478476-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 29920012-C-G

37478476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 29920012-C-T

37478484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 29920020-T-C

37478496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 29920032-C-T

37478614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29920114-G-T

http://identifiers.org/hco/6/GRCh38#37479022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29920365-C-A

37479022-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29920365-C-G

37479022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29920365-C-T

http://identifiers.org/hco/6/GRCh38#37479032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29920366-C-A

37479069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29920399-A-G

37479086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29920416-G-A

37479086-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29920416-G-C

37479086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29920416-G-T

37479124-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29920439-T-G

37479321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29920581-A-G

http://identifiers.org/hco/6/GRCh38#37479327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29920587-C-A

37479327-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29920587-C-G

37479327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29920587-C-T

37479617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29920744-A-G

37479767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29920883-A-G

37479863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29920959-G-T

http://identifiers.org/hco/6/GRCh38#37480266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29921367-C-A

37480266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 29921367-C-T

http://identifiers.org/hco/6/GRCh38#37480580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29921608-C-A

37480580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 29921608-C-T

37480582-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 29921610-T-A

37480582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 29921610-T-C

http://identifiers.org/hco/6/GRCh38#37480901-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29921816-C-A

37480901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 29921816-C-T

37480905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 29921820-G-A

37480905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 29921820-G-T

http://identifiers.org/hco/6/GRCh38#37481445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29922272-C-A

37481445-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 29922272-C-G

37481445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 29922272-C-T

http://identifiers.org/hco/6/GRCh38#37481472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29922299-C-A

37481472-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 29922299-C-G

37481472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 29922299-C-T

37482010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29922676-T-C

37482100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29922711-G-A

37482239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29922786-C-T

http://identifiers.org/hco/6/GRCh38#37482417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29922886-C-A

37482458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: intron variant
orthologous variants: 29922925-G-T

http://identifiers.org/hco/6/GRCh38#37482565-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29923028-A-C

37482588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: 3 prime UTR variant
orthologous variants: 29923049-G-A

http://identifiers.org/hco/6/GRCh38#37482591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29923052-C-A

37482591-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: 3 prime UTR variant
orthologous variants: 29923052-C-G

37482591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: 3 prime UTR variant
orthologous variants: 29923052-C-T

37482652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21077
most severe consequence: 3 prime UTR variant
orthologous variants: 29923107-G-T