15002615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 43390747-G-A

15002615-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 43390747-G-T

15002906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: missense variant
orthologous variants: 43391023-C-T

15002973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: synonymous variant
orthologous variants: 43391087-G-A

15003372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: synonymous_variant, undefined
orthologous variants: 43391483-G-A

15003372-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: synonymous_variant, undefined
orthologous variants: 43391483-G-C

15003372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: synonymous_variant, undefined
orthologous variants: 43391483-G-T

http://identifiers.org/hco/4/GRCh38#15003384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43391495-C-A

15003384-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: missense variant
orthologous variants: 43391495-C-G

15003384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: synonymous variant
orthologous variants: 43391495-C-T

15003401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: missense variant
orthologous variants: 43391512-A-G

15003401-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: missense variant
orthologous variants: 43391512-A-T

http://identifiers.org/hco/4/GRCh38#15003466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43391577-C-A

15003466-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: missense variant
orthologous variants: 43391577-C-G

15003466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: missense variant
orthologous variants: 43391577-C-T

15003652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: missense variant
orthologous variants: 43391766-A-G

15003675-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: synonymous variant
orthologous variants: 43391789-T-A

15003675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: synonymous variant
orthologous variants: 43391789-T-C

15003675-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: synonymous variant
orthologous variants: 43391789-T-G

http://identifiers.org/hco/4/GRCh38#15003732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43391837-C-A

15003732-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: synonymous variant
orthologous variants: 43391837-C-G

15003732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: synonymous variant
orthologous variants: 43391837-C-T

15003909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: synonymous variant
orthologous variants: 43392011-G-A

15003909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: synonymous variant
orthologous variants: 43392011-G-T

15004155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: synonymous variant
orthologous variants: 43392260-T-C

15004155-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: synonymous variant
orthologous variants: 43392260-T-G

http://identifiers.org/hco/4/GRCh38#15004213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43392309-C-A

15004213-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: missense variant
orthologous variants: 43392309-C-G

15004213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: missense variant
orthologous variants: 43392309-C-T

15004589-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron variant
orthologous variants: 43392461-G-C

http://identifiers.org/hco/4/GRCh38#15004619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43392482-C-A

15004803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron variant
orthologous variants: 43392573-G-A

15004803-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron variant
orthologous variants: 43392573-G-C

15004803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron variant
orthologous variants: 43392573-G-T

15004804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron variant
orthologous variants: 43392574-G-T

15004805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron variant
orthologous variants: 43392575-G-A

15004805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron variant
orthologous variants: 43392575-G-T

http://identifiers.org/hco/4/GRCh38#15005268-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43392785-C-A

15006219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43393659-G-A

15006363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43393796-C-T

15006419-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43393852-T-A

15006419-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43393852-T-G

15006787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43394205-C-T

15006872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43394310-A-G

15007179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43394527-A-G

15007198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43394546-G-A

15007198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43394546-G-T

http://identifiers.org/hco/4/GRCh38#15007262-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43394607-A-C

15007262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43394607-A-G

15007262-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43394607-A-T

http://identifiers.org/hco/4/GRCh38#15007361-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43394706-A-C

15007385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 43394730-T-C

15007385-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43394730-T-G

15007386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43394731-G-A

http://identifiers.org/hco/4/GRCh38#15007409-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43394754-A-C

15007448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 43394793-A-G

15007463-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43394808-T-A

http://identifiers.org/hco/4/GRCh38#15007523-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43394868-A-C

http://identifiers.org/hco/4/GRCh38#15007625-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43394970-A-C

15007625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43394970-A-G

http://identifiers.org/hco/4/GRCh38#15007677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43395029-C-A

15007677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43395029-C-T

15007880-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43395215-T-A

15007880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43395215-T-C

15008011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43395343-G-A

http://identifiers.org/hco/4/GRCh38#15008444-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43395779-A-C

15008444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43395779-A-G

15008500-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43395835-T-A

15008500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43395835-T-C

http://identifiers.org/hco/4/GRCh38#15008506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43395841-C-A

15008506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43395841-C-T

15008879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43396210-G-A

15008879-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43396210-G-C

15008879-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43396210-G-T

15008927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43396265-A-G

15009109-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43396378-G-C

15009401-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43396660-T-G

15009468-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43396725-T-A

15009468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43396725-T-C

15009518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43396778-G-A

15009565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43396804-A-G

15009566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43396805-T-C

15009917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43397094-G-A

15010072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43397256-T-C

15010107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43397293-A-G

15010134-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43397320-G-C

15010160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43397342-T-C

15010289-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43397452-C-G

15010336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43397498-C-T

15010361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43397534-A-G

15010362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43397535-T-C

15010430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43397592-G-A

http://identifiers.org/hco/4/GRCh38#15010557-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43397680-A-C

15010557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43397680-A-G

15010889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43397975-G-A

15012054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43399069-C-T

15012088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43399103-A-G

http://identifiers.org/hco/4/GRCh38#15012144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43399146-C-A

15012144-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43399146-C-G

15013331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43399470-T-C

15013516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43399649-A-G

15014565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43399870-A-G

15014586-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43399881-C-G

15014730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43400003-C-T

15014803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43400073-A-G

15014837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43400108-A-G

15014963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43400222-T-C

15015290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43400510-C-T

15015474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43400687-A-G

15015514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43400731-A-G

15016384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43401203-A-G

http://identifiers.org/hco/4/GRCh38#15016402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43401222-C-A

15017069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43401806-A-G

15017088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43401830-A-G

http://identifiers.org/hco/4/GRCh38#15017128-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43401870-A-C

15017128-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43401870-A-T

http://identifiers.org/hco/4/GRCh38#15017146-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43401888-A-C

15017308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43402042-T-C

15017458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43402141-G-A

15017765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43402331-G-A

15017814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 43402383-G-T

15018140-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43402681-T-G

15018530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43402976-G-A

15018534-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43402980-C-G

15018543-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43402989-G-C

15018550-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43402996-G-C

15018640-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43403203-T-G

15018815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43403355-G-T

15018909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43403439-G-A

15018909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43403439-G-T

15019205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43403645-G-A

15019323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43403751-C-T

15019324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43403752-C-T

15019433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43403850-A-G

15019542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43403953-C-T

15019755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43404118-G-T

15019910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43404250-G-A

http://identifiers.org/hco/4/GRCh38#15020109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43404440-C-A

15020129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43404473-A-G

15020156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43404512-A-G

15020412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43404766-C-T

http://identifiers.org/hco/4/GRCh38#15020455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43404799-C-A

15020466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43404811-T-C

15020483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43404828-G-A

15020498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43404841-T-C

15020630-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43404942-G-C

15020633-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43404947-T-A

15020653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43404967-A-G

http://identifiers.org/hco/4/GRCh38#15020654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43404968-C-A

15020754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43405052-C-T

15020774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43405072-G-T

15020817-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43405119-C-G

15021302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43405564-A-G

15021303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43405565-G-A

15021780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43406032-A-G

15021785-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43406037-C-G

http://identifiers.org/hco/4/GRCh38#15022036-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43406273-A-C

15022043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43406277-A-G

15022329-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43406532-C-G

15022564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43406982-G-A

15022740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43407289-A-G

15022751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43407300-A-G

http://identifiers.org/hco/4/GRCh38#15023327-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43407844-A-C

15023605-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43408083-A-T

15023711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43408156-A-G

15023778-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43408199-A-T

15023805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43408204-A-G

15023805-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43408204-A-T

15025078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43409658-C-T

15025303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43409912-A-G

15025528-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43410127-C-G

15025631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43410235-C-T

15025720-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43410302-G-C

15025811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43410381-G-A

15025844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43410415-C-T

http://identifiers.org/hco/4/GRCh38#15025872-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43410430-A-C

15026943-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43411222-T-G

15027199-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43413549-T-G

15027534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 43413830-T-C

15028012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43414222-T-C

15028211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43414494-G-A

15028317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43414695-G-T

15028360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43414735-C-T

15028802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43415138-G-A

15028802-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43415138-G-C

15028821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43415154-G-A

15028913-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43415236-G-C

15029960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43416434-G-A

15029960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43416434-G-T

15030114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43416527-G-A

15030157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43416570-G-T

15030183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43416593-A-G

15030183-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43416593-A-T

15030513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43416876-A-G

15030776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43417095-A-G

15030798-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43417112-A-T

15031004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43417258-A-G

15031055-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43417303-A-T

http://identifiers.org/hco/4/GRCh38#15031083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43417331-C-A

15031083-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43417331-C-G

15031264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43417496-G-A

15031289-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43417516-A-T

15031438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43417644-T-C

15031900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43418076-G-A

15031959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43418116-A-G

15032905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43418855-A-G

15032915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43418866-C-T

15033007-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43418950-T-G

15033013-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43418956-T-G

15033025-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43418969-T-G

15033118-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43419032-T-G

15033652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43419694-T-C

15033656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43419698-G-A

15033706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43419744-A-G

15033972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43419945-G-A

15034045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43420017-G-A

http://identifiers.org/hco/4/GRCh38#15034563-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43420854-A-C

15034597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43420885-G-A

15034598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43420886-C-T

15034719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43420979-G-A

15034719-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43420979-G-C

15034946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43421135-T-C

15034982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43421171-A-G

15035120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43421278-G-A

15035157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43421321-T-C

15035186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43421350-A-G

15035598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43421689-T-C

15035600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43421691-A-G

15035932-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43421996-C-G

15035937-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43422001-T-G

15035955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43422023-G-A

15036073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43422143-A-G

15036590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43422731-G-A

15036800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43422928-G-A

15036816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43422943-G-T

15037168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43423151-T-C

15037588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43423507-T-C

http://identifiers.org/hco/4/GRCh38#15037625-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43423543-A-C

15037625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43423543-A-G

15037627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43423545-T-C

15037753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43423632-C-T

15037994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43423889-A-G

15037994-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43423889-A-T

15038150-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43424248-C-G

15038214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43424312-C-T

15038324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43424433-C-T

15038452-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43424569-A-T

15038494-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43424609-A-T

15039072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43424880-A-G

15039091-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43424893-C-G

15039248-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43425021-A-T

15039283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43425055-A-G

15039675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43425430-C-T

15040204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43425920-C-T

15040326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43426082-G-A

15040326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43426082-G-T

15040389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43426137-G-A

15040395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43426143-G-T

15040658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43426411-G-A

http://identifiers.org/hco/4/GRCh38#15040905-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43426619-A-C

15040905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43426619-A-G

http://identifiers.org/hco/4/GRCh38#15040943-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43426658-A-C

15040943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43426658-A-G

15040944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43426659-G-A

15041078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43426757-A-G

15041270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43426942-A-G

15042078-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43427398-T-A

15042081-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43427401-A-T

http://identifiers.org/hco/4/GRCh38#15042172-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43427459-A-C

15042172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43427459-A-G

15042176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43427463-A-G

15042421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43427691-C-T

15042423-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43427693-T-A

15042647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43427885-G-A

15042647-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43427885-G-C

15042656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43427894-A-G

15042746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43427988-A-G

15042763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43428005-G-A

15042885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43428114-A-G

15043430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43428643-G-A

15043430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43428643-G-T

15043552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43428757-T-C

15043609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43428814-C-T

15043627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43428832-C-T

15043735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43428939-G-A

15043868-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43429056-T-G

15044073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43429211-A-G

15044195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43429330-G-A

http://identifiers.org/hco/4/GRCh38#15044297-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43429436-A-C

15044720-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43429790-G-C

15049408-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43431019-T-A

15049578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43431198-C-T

15049595-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43431218-T-G

15049692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43431457-G-A

15049698-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43431464-T-A

15050461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43432951-G-A

15050702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43433201-T-C

15050808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43433298-C-T

15050813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43433303-C-T

15050868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43433351-C-T

15051088-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43433538-C-G

15051111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43433561-A-G

http://identifiers.org/hco/4/GRCh38#15051123-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43433573-A-C

15051123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43433573-A-G

15051123-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43433573-A-T

15051441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43433765-C-T

15051554-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43433847-C-G

15051572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43433869-A-G

15051618-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43433921-C-G

15051618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43433921-C-T

15051677-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43433981-G-C

http://identifiers.org/hco/4/GRCh38#15051696-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43434000-A-C

http://identifiers.org/hco/4/GRCh38#15051851-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43434183-A-C

15051913-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43434240-T-G

15051916-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43434243-A-T

15052258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43434608-A-G

15052262-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43434612-A-T

http://identifiers.org/hco/4/GRCh38#15052303-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43434657-A-C

15052303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43434657-A-G

15052346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43434698-T-C

15052354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43434705-T-C

15052359-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43434710-A-T

15052381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43434740-T-C

15052381-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43434740-T-G

15052400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43434759-G-A

15052400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43434759-G-T

http://identifiers.org/hco/4/GRCh38#15052542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43434902-C-A

15052580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 43434940-T-C

15052630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43434968-A-G

http://identifiers.org/hco/4/GRCh38#15052634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43434972-C-A

15052634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43434972-C-T

15052644-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43434982-T-A

15052644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43434982-T-C

15052644-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43434982-T-G

15053736-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43435559-C-G

15053742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43435565-T-C

15053871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43435694-A-G

http://identifiers.org/hco/4/GRCh38#15053887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43435710-C-A

15053887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43435710-C-T

15053896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43435714-T-C

15054001-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43435817-T-G

15054099-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43435919-T-G

http://identifiers.org/hco/4/GRCh38#15054100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43435920-C-A

15054100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43435920-C-T

15054283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43436091-A-G

15057065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43437895-G-A

15057065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43437895-G-T

15059573-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43438864-C-G

15059575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43438866-G-A

15059724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43438951-G-T

15059752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43438976-A-G

15059790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43439010-A-G

15059801-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43439021-T-A

15059801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43439021-T-C

15059985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43439200-C-T

15060103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43439410-G-A

15060201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43439521-G-A

15060384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43439716-G-A

15060384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43439716-G-T

15060662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43439932-A-G

15060684-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43439954-A-T

15060890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43440134-G-A

15060890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43440134-G-T

http://identifiers.org/hco/4/GRCh38#15061038-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43440273-A-C

15061038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43440273-A-G

15061181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43440410-A-G

15061223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43440455-G-T

15061361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43440557-T-C

15061672-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43440877-T-G

15061791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43440983-G-A

15061861-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43441073-T-A

15061922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43441165-G-A

15061922-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43441165-G-C

15061929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43441175-G-A

15061929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43441175-G-T

15061938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43441187-T-C

http://identifiers.org/hco/4/GRCh38#15061941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43441190-C-A

http://identifiers.org/hco/4/GRCh38#15062011-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43441228-A-C

15062011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43441228-A-G

15062056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43441258-G-A

15062075-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 43441276-C-G

15062475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43441640-G-A

15062637-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43441810-G-C

15062654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43441827-G-A

15062724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43441882-A-G

15065475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43442280-C-T

15065687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43442478-A-G

15065749-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43442539-C-G

15065749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43442539-C-T

15065943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43442724-G-A

http://identifiers.org/hco/4/GRCh38#15066006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43442908-C-A

15066006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43442908-C-T

15066059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43442954-G-A

15066059-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43442954-G-C

15066059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43442954-G-T

15066150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 43443059-A-G

15066399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 43443308-T-C

15066405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 43443314-A-G

http://identifiers.org/hco/4/GRCh38#15067031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43443938-C-A

15067031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43443938-C-T

15067168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43444072-C-T

http://identifiers.org/hco/4/GRCh38#15067594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43444504-C-A

15067633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43444542-A-G

15068422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43445319-G-A

15068422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43445319-G-T

15068473-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43445370-G-C

http://identifiers.org/hco/4/GRCh38#15068842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43445745-C-A

15068842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43445745-C-T

15068921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43445825-G-T

15070152-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21745
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43447068-T-G