841701-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 25483129-C-G

841701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 25483129-C-T

http://identifiers.org/hco/9/GRCh38#841720-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#25483148-A-C

841720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 25483148-A-G

842003-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 25483376-C-G

842099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 25483472-G-A

842099-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 25483472-G-C

842099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 25483472-G-T

842384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25483625-A-G

http://identifiers.org/hco/9/GRCh38#842475-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#25483645-A-C

842475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25483645-A-G

842475-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25483645-A-T

842485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25483655-C-T

842512-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25483673-A-T

842541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25483699-C-T

842584-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25483736-C-G

842584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25483736-C-T

842598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25483741-T-C

842603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25483746-A-G

http://identifiers.org/hco/9/GRCh38#842621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#25483764-C-A

842621-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25483764-C-G

842621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25483764-C-T

842630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25483773-C-T

842641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25483779-G-A

842655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25483795-G-A

842655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25483795-G-T

http://identifiers.org/hco/9/GRCh38#842745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#25483850-C-A

842745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25483850-C-T

842760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25483863-C-T

842782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25483884-G-A

842782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25483884-G-T

http://identifiers.org/hco/9/GRCh38#842821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#25483923-C-A

843073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25484139-C-T

843118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25484176-C-T

843125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25484183-T-C

843303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25484273-G-T

843318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25484288-G-T

843364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25484334-G-A

843364-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25484334-G-C

843480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25484433-T-C

843553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 25484509-A-G

843615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25484573-A-G

843685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25484640-T-C

843796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25484770-T-C

http://identifiers.org/hco/9/GRCh38#843861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#25484832-C-A

844017-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25484974-C-G

844284-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25485190-C-G

844284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25485190-C-T

844293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25485199-A-G

844331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25485237-T-C

844349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25485249-A-G

844471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25485399-T-C

http://identifiers.org/hco/9/GRCh38#844473-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#25485401-A-C

844555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25485514-T-C

http://identifiers.org/hco/9/GRCh38#844605-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#25485563-A-C

846375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25486356-A-G

846391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25486371-G-A

846391-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25486371-G-C

846391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25486371-G-T

846399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25486379-T-C

846442-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25486431-T-A

846928-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25487013-C-G

846933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25487018-G-A

http://identifiers.org/hco/9/GRCh38#846942-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#25487027-A-C

846942-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25487027-A-T

847013-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 25487097-C-G

847013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 25487097-C-T

847034-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 25487118-C-G

847034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 25487118-C-T

847073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 25487157-G-A

847090-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 25487174-G-C

847109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 25487193-A-G

847109-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 25487193-A-T

847134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 25487218-G-A

847134-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 25487218-G-C

847235-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25487327-T-A

847235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25487327-T-C

847235-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25487327-T-G

http://identifiers.org/hco/9/GRCh38#847269-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#25487355-A-C

847269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25487355-A-G

847269-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25487355-A-T

http://identifiers.org/hco/9/GRCh38#847295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#25487381-C-A

847295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25487381-C-T

847363-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25487440-G-C

847460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25487525-G-A

847460-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25487525-G-C

847539-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25487610-C-G

847539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25487610-C-T

847598-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25487670-G-C

847787-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25487908-G-C

850141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25489740-A-G

850353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25489940-G-A

850469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25490057-G-A

851577-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25491816-C-G

851630-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25491872-T-G

851768-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25492003-C-G

851768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25492003-C-T

851887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25492109-C-T

851913-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25492135-C-G

851913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25492135-C-T

852394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25492259-T-C

http://identifiers.org/hco/9/GRCh38#852453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#25492311-C-A

852453-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25492311-C-G

852453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25492311-C-T

http://identifiers.org/hco/9/GRCh38#852510-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#25492354-A-C

852521-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25492368-C-G

852545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25492389-A-G

855403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25494738-G-A

855438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25494775-A-G

855438-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25494775-A-T

855569-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25494901-C-G

858169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25497222-C-T

858188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25497240-A-G

858431-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25497431-G-C

858444-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25497444-T-A

858464-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25497458-C-G

858490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25497483-C-T

859425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25498350-G-A

859425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25498350-G-T

859800-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25498721-G-C

859950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25498879-T-C

859971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25498900-C-T

860383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25499001-A-G

860470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25499069-G-A

860524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25499109-C-T

860641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25499200-A-G

860716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25499266-G-A

860900-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25499389-G-C

861015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25499481-A-G

861026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25499492-G-A

864118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25500853-G-A

864170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25500906-G-A

http://identifiers.org/hco/9/GRCh38#865064-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#25502205-C-A

865085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25502226-A-G

http://identifiers.org/hco/9/GRCh38#865187-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#25502341-A-C

865187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25502341-A-G

http://identifiers.org/hco/9/GRCh38#865192-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#25502346-A-C

865259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25502418-A-G

865337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25502482-G-T

865386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25502524-A-G

865407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25502545-G-A

865578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25502700-C-T

865702-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25502811-C-G

866344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25503408-C-T

866354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25503418-A-G

866358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25503422-G-A

866358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25503422-G-T

http://identifiers.org/hco/9/GRCh38#866422-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#25503458-A-C

866422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25503458-A-G

866635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25503667-G-A

866635-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25503667-G-C

866691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25503723-C-T

866701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25503732-T-C

866741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25503760-A-G

http://identifiers.org/hco/9/GRCh38#866767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#25503786-C-A

866776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25503795-G-A

http://identifiers.org/hco/9/GRCh38#866825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#25503825-C-A

866850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25503846-G-A

866895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25503913-C-T

866978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25503998-G-A

867424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25504435-T-C

867464-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25504481-C-G

867464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25504481-C-T

867485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25504511-G-A

867496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25504522-G-T

867675-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25504705-G-C

867758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25504786-G-A

867956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25505040-G-A

http://identifiers.org/hco/9/GRCh38#868014-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#25505181-A-C

868014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25505181-A-G

868055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25505210-G-A

868055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25505210-G-T

868139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25505287-G-A

868139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25505287-G-T

868306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25505486-T-C

868306-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25505486-T-G

http://identifiers.org/hco/9/GRCh38#868424-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#25505663-A-C

868461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25505701-T-C

http://identifiers.org/hco/9/GRCh38#868529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#25505769-C-A

868529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25505769-C-T

868532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25505772-A-G

868556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25505795-G-A

868556-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25505795-G-C

868556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25505795-G-T

http://identifiers.org/hco/9/GRCh38#868562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#25505801-C-A

868603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25505829-G-T

868630-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25505848-G-C

869149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25506503-T-C

869185-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25506568-C-G

869214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25506596-G-A

869222-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25506604-C-G

869259-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25506638-C-G

869308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25506675-T-C

869343-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25506710-G-C

869423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25506743-C-T

869565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25506886-C-T

869571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25506892-A-G

869684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25507005-A-G

870643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25507520-G-A

870655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25507532-G-T

870672-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25507562-C-G

870672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25507562-C-T

870692-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25507582-A-T

http://identifiers.org/hco/9/GRCh38#870698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#25507588-C-A

870698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25507588-C-T

http://identifiers.org/hco/9/GRCh38#870708-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#25507598-A-C

870708-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25507598-A-T

870737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25507629-G-A

870737-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25507629-G-C

870737-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25507629-G-T

870796-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25507679-C-G

870828-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25507709-C-G

http://identifiers.org/hco/9/GRCh38#870835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#25507716-C-A

870857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25507737-G-A

870862-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25507742-C-G

875806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25509088-A-G

875827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25509110-A-G

875827-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25509110-A-T

875843-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25509153-A-T

http://identifiers.org/hco/9/GRCh38#875850-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#25509160-A-C

875999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25509338-C-T

877440-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25509987-C-G

http://identifiers.org/hco/9/GRCh38#877600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#25510113-C-A

877612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25510125-C-T

877783-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25514024-A-T

877857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25514103-A-G

877866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25514112-C-T

877898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25514144-A-G

877900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25514146-A-G

877922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25514175-A-G

http://identifiers.org/hco/9/GRCh38#877969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#25514220-C-A

878131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25514381-G-T

http://identifiers.org/hco/9/GRCh38#878212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#25514462-C-A

878212-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25514462-C-G

878212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25514462-C-T

878272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25514521-C-T

878279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25514529-G-A

878279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25514529-G-T

878471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25514714-T-C

878540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25514783-A-G

878577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25514820-G-A

878585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25514837-T-C

878780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25515030-C-T

878864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25515305-T-C

879026-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25515445-A-T

879055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25515485-G-A

879055-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25515485-G-C

879098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25515509-C-T

879250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25515645-G-A

879296-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25515690-T-A

883914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25519045-G-T

883955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25519080-A-G

884025-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25519126-T-G

884068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25519163-T-C

884271-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25519333-C-G

884453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25519508-C-T

884477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25519531-C-T

884504-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25519558-A-T

884621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25519642-T-C

884700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25519706-G-A

884707-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25519714-A-T

885737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25519828-T-C

885742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25519833-C-T

885755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25519846-T-C

885806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25519874-C-T

885812-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25519879-C-G

885952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25519964-C-T

885999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25520007-T-C

886070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25520074-T-C

889849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

889850-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-C

889919-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-T

890010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

890084-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-A

890084-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-G

890419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

890419-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-C

890436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

http://identifiers.org/hco/9/GRCh38#890442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-A

890442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

http://identifiers.org/hco/9/GRCh38#890625-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-C

890627-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-G

890688-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-C

891948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25521800-G-T

891982-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25521833-G-C

891982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25521833-G-T

892235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25522218-G-A

892235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25522218-G-T

892278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25522258-T-C

892376-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25522332-A-T

892430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25522401-C-T

892434-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25522405-T-G

892443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25522418-C-T

892459-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25522434-C-G

892493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25522467-C-T

892610-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25522571-C-G

892658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25522613-G-A

892659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25522614-C-T

892666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25522621-C-T

893548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25522773-A-G

893586-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25522813-G-C

893671-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25522868-C-G

893774-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25522967-G-C

893774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25522967-G-T

893850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25523054-A-G

http://identifiers.org/hco/9/GRCh38#893905-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#25523176-A-C

893905-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 25523176-A-T

893919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 25523190-T-C

894197-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: non_coding_transcript_exon_variant, splice_donor_variant, undefined
orthologous variants: 25523468-T-G

894227-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 25523487-G-C

894240-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 25523500-C-G

894240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 25523500-C-T

894244-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 25523504-T-G

http://identifiers.org/hco/9/GRCh38#894257-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#25523521-A-C

894257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 25523521-A-G

http://identifiers.org/hco/9/GRCh38#894319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#25523540-C-A

894319-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 25523540-C-G

894320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 25523541-A-G

http://identifiers.org/hco/9/GRCh38#894350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#25523551-C-A

894350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 25523551-C-T

894367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 25523568-G-A

http://identifiers.org/hco/9/GRCh38#894466-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#25523657-A-C

894466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 25523657-A-G

http://identifiers.org/hco/9/GRCh38#894485-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#25523678-A-C

894489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 25523682-T-C

894526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 25523718-G-A

894526-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 25523718-G-C

894526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 25523718-G-T

http://identifiers.org/hco/9/GRCh38#894622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#25523801-C-A

894622-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 25523801-C-G

894622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 25523801-C-T

http://identifiers.org/hco/9/GRCh38#897979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#25525271-C-A

897979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25525271-C-T

898040-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25525322-A-T

898204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25525487-C-T

898254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25525529-G-A

898254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25525529-G-T

http://identifiers.org/hco/9/GRCh38#898271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#25525546-C-A

898503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25526164-T-C

898539-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25526201-C-G

898631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25526249-C-T

899216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25526575-A-G

899447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, undefined
orthologous variants: 25526834-G-A

899767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25527147-G-A

899842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25527220-C-T

899887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25527266-G-T

899893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25527272-C-T

899910-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, undefined
orthologous variants: 25527289-G-C

899970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25527343-C-T

900224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25527681-C-T

900245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25527702-C-T

900251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25527708-C-T

900368-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25527841-C-G

900368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25527841-C-T

900500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25527943-T-C

900502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25527945-C-T

900504-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25527949-G-C

900778-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25528249-G-C

903679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25529458-G-A

903679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25529458-G-T

903722-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25529477-A-T

903801-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25529557-A-T

903802-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25529558-T-A

903886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25529640-G-A

903940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25529689-T-C

903959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25529708-A-G

904054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, undefined
orthologous variants: 25529797-C-T

904469-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25530158-G-C

904594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25530195-T-C

904739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25530281-G-A

904889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25530370-C-T

905098-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25530459-T-A

905107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25530468-A-G

905223-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25530579-G-C

905283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25530630-A-G

905472-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25530857-C-G

905742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25531214-T-C

905805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25531274-G-A

905849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25531318-G-A

905929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25531394-T-C

905967-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25531431-G-C

905995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25531458-A-G

906034-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25531505-C-G

906034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25531505-C-T

906053-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25531524-T-A

906053-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25531524-T-G

906151-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25531560-T-G

906159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25531568-C-T

906205-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25531615-T-A

906205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25531615-T-C

http://identifiers.org/hco/9/GRCh38#906318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#25531737-C-A

906807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25532233-A-G

906981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25532398-C-T

906988-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25532405-C-G

906988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25532405-C-T

906990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25532407-A-G

906994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25532411-T-C

907042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25532453-T-C

http://identifiers.org/hco/9/GRCh38#907487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#25533469-C-A

907626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25533608-T-C

907968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25533834-C-T

910845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25534643-C-T

910905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25534699-G-A

910906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25534700-G-A

910967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25534814-C-T

911043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25534864-T-C

911052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25534873-G-A

911052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25534873-G-T

911086-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25534904-G-C

911111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25534930-C-T

912358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25535512-A-G

912359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25535513-A-G

912425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25535582-G-A

912467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25535619-A-G

912775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25536085-A-G

912777-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25536087-C-G

912787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25536097-T-C

912856-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25536165-T-G

913203-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25536471-G-C

http://identifiers.org/hco/9/GRCh38#913208-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#25536476-A-C

913315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25536581-G-A

913337-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25536606-C-G

913404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25536660-T-C

916738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25537206-A-G

916738-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25537206-A-T

916870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: synonymous variant
orthologous variants: 25537338-T-C

917013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25537468-A-G

923553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25542323-T-C

923593-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25542361-G-C

923620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25542388-G-A

923917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25542834-C-T

923968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25542883-G-T

924433-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25543010-T-A

924548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25543129-G-T

924626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25543248-T-C

924669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25543302-T-C

924747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25543366-T-C

924962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25543569-G-A

924997-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25543607-A-T

925055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25543666-A-G

925200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25543769-C-T

http://identifiers.org/hco/9/GRCh38#925304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#25543855-C-A

925304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25543855-C-T

925329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25543879-A-G

925578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25544122-C-T

925650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25544184-A-G

925854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25544393-G-A

925972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25544512-G-A

925972-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25544512-G-C

926054-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25544566-C-G

926156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25544664-C-T

926159-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25544667-C-G

926159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25544667-C-T

http://identifiers.org/hco/9/GRCh38#926183-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#25544681-A-C

926296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25544760-G-A

926532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25545053-A-G

926586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25545108-C-T

926975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25545459-C-T

927013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25545496-C-T

927151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25545611-C-T

927160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25545620-G-A

927160-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25545620-G-T

927194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25545654-G-A

927221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25545677-G-A

927656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25546114-G-A

http://identifiers.org/hco/9/GRCh38#928537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#25546948-C-A

928537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25546948-C-T

928542-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25546953-G-C

928601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25547010-T-C

929444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25547384-G-T

929928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, undefined
orthologous variants: 25548067-G-T

930027-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25548155-C-G

930059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25548187-C-T

930093-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25548217-T-G

930159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25548260-C-T

930979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25548448-T-C

931129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25548679-G-A

931129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25548679-G-T

931602-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25549096-G-C

931677-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25549249-C-G

931866-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25549432-G-C

931885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25549449-G-A

931913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25549477-G-A

931913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25549477-G-T

931930-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25549494-C-G

931930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25549494-C-T

932039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25549586-T-C

932057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25549603-A-G

932070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25549616-G-A

932081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25549627-T-C

http://identifiers.org/hco/9/GRCh38#932171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#25549705-C-A

http://identifiers.org/hco/9/GRCh38#932200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#25549725-C-A

932201-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25549726-A-T

932251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25549763-A-G

932582-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25550081-T-A

932721-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25550176-C-G

933732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25551561-T-C

933861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25551697-C-T

http://identifiers.org/hco/9/GRCh38#934014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#25551843-C-A

934369-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25552154-T-A

934369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25552154-T-C

934757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25552363-C-T

934809-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25552407-G-C

http://identifiers.org/hco/9/GRCh38#934831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#25552428-C-A

934835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25552432-T-C

935034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25552569-G-A

935205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25552712-A-G

935447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron_variant, undefined
orthologous variants: 25552960-C-T

935624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25553132-G-T

http://identifiers.org/hco/9/GRCh38#935699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#25553206-C-A

935699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25553206-C-T

935731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25553238-C-T

935734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25553241-C-T

935900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25553413-A-G

935988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25553482-G-A

935988-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25553482-G-C

936074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25553573-C-T

936124-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25553630-T-G

936398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25553882-G-A

936398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25553882-G-T

941832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25556410-T-C

941866-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25556444-T-G

941892-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25556468-T-A

941892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25556468-T-C

942109-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25556680-G-C

942197-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25556768-T-G

942256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25556836-A-G

942656-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25557157-A-T

942661-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25557162-T-A

942661-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25557162-T-G

942672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25557177-G-T

942716-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25557217-C-G

942716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25557217-C-T

942729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25557230-G-T

943022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25557630-A-G

http://identifiers.org/hco/9/GRCh38#943026-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#25557634-A-C

943111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25557717-T-C

943164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25557769-A-G

943197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25557802-C-T

943343-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25557947-C-G

http://identifiers.org/hco/9/GRCh38#943567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#25558170-C-A

943570-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25558173-C-G

943595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25558195-T-C

943640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25558231-T-C

943655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25558246-G-A

943747-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25558329-C-G

943755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25558337-G-A

943769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25558350-A-G

943811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25558392-G-A

http://identifiers.org/hco/9/GRCh38#943966-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#25559040-A-C

943984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25559058-G-T

944027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25559096-A-G

944115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25559166-G-A

944230-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25559259-G-C

944410-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25559470-T-A

944670-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25559762-A-T

944753-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25559840-G-C

944819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25559911-A-G

944849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25559930-A-G

944871-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25559956-G-C

944936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25560025-A-G

944975-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25560058-G-C

944975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25560058-G-T

945045-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25560112-T-A

945075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25560135-T-C

945119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25560184-A-G

945612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25560768-G-T

945685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25560865-C-T

http://identifiers.org/hco/9/GRCh38#945735-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#25560914-A-C

945772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25560941-G-A

945772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25560941-G-T

945787-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25560956-A-T

945810-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25560977-A-T

945857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25561005-T-C

945873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25561021-A-G

945902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25561050-T-C

945916-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25561061-G-C

945951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25561100-T-C

946009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25561147-A-G

946180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25561353-G-T

946181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25561354-C-T

946184-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25561357-T-A

946239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25561435-A-G

946462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25561623-A-G

946462-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25561623-A-T

946473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25561636-C-T

946568-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25561734-T-A

http://identifiers.org/hco/9/GRCh38#946586-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#25561752-A-C

946736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25562266-G-T

946817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25562335-C-T

947059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25562445-C-T

947092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25562478-G-A

947133-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25562519-T-G

947648-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25562725-G-C

947648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25562725-G-T

947663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25562737-G-A

947705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25562746-C-T

947869-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25562900-C-G

948238-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25563259-C-G

949592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25564610-G-T

949666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25564642-C-T

949772-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25564717-T-G

949871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25564802-G-A

949911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25564848-A-G

949980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25564919-C-T

949990-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25564926-C-G

950013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25564949-C-T

950019-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25564961-A-T

950133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25565063-G-T

950201-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25565137-T-G

950280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25565200-A-G

950733-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25565587-A-T

950921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25565783-A-G

950991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25566011-C-T

http://identifiers.org/hco/9/GRCh38#951050-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#25566065-A-C

951050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25566065-A-G

951237-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25566260-G-C

951294-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25566301-A-T

951299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25566318-T-C

951352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25566479-T-C

951444-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25566656-C-G

951444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25566656-C-T

951447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25566659-G-T

951506-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25566705-G-C

951530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25566728-G-A

951633-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25566818-T-A

951779-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25566942-A-T

951928-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25567052-G-C

951928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25567052-G-T

951979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25567098-C-T

952009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25567124-C-T

http://identifiers.org/hco/9/GRCh38#952058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#25567168-C-A

952257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25567505-C-T

952279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25567534-G-A

952291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25567546-G-T

952498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25567748-C-T

952633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25568124-G-T

952670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25568162-A-G

952761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25568250-A-G

952982-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25568444-C-G

953034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25568496-G-A

953034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25568496-G-T

953062-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25568524-T-A

955097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25569181-G-T

955207-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25569256-C-G

955825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25569667-T-C

955842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25569687-G-A

http://identifiers.org/hco/9/GRCh38#956016-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#25569862-A-C

956175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25570023-G-A

956374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25570220-A-G

956374-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25570220-A-T

956509-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25570253-A-T

http://identifiers.org/hco/9/GRCh38#956555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#25570264-C-A

956562-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25570271-T-A

956562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25570271-T-C

http://identifiers.org/hco/9/GRCh38#956577-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#25570286-A-C

956895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25570481-G-A

957110-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25570578-T-A

957292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25570695-A-G

957310-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25570713-C-G

957328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25570731-C-T

957511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25570895-T-C

957511-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25570895-T-G

http://identifiers.org/hco/9/GRCh38#957517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#25570902-C-A

957531-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25570916-C-G

957555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25570940-T-C

957645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25571025-T-C

957649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25571028-T-C

http://identifiers.org/hco/9/GRCh38#958176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#25571228-C-A

958176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25571228-C-T

958193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25571245-G-A

958193-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25571245-G-C

958232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25571283-A-G

958287-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25571339-A-T

959017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25572362-T-C

959864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25573080-G-T

960238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25573395-C-T

960537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25573646-T-C

962900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25575532-C-T

962901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25575533-C-T

962937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25575562-A-G

963532-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25576141-T-G

963570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25576178-T-C

964107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25576715-C-T

964108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25576716-G-A

964283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25576914-T-C

964466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25577045-T-C

964483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25577054-T-C

964483-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25577054-T-G

964551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25577104-T-C

http://identifiers.org/hco/9/GRCh38#964700-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#25577227-A-C

964891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25577420-A-G

964972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25577499-G-A

964991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25577533-C-T

965013-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25577569-T-G

965117-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25577656-G-C

965176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25577704-C-T

965200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25577728-A-G

965206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25577735-A-G

http://identifiers.org/hco/9/GRCh38#965265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#25577802-C-A

965265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25577802-C-T

965298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25577818-A-G

965442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25577950-A-G

965505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25577992-C-T

965517-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25578005-A-T

966086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25578460-A-G

966089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25578463-T-C

966142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25578535-C-T

966590-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25579152-T-G

966673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25579224-T-C

966746-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25579296-A-T

967123-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25579672-A-T

967170-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25579718-C-G

967457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25579994-C-T

967649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25580182-A-G

http://identifiers.org/hco/9/GRCh38#967704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#25580228-C-A

967704-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25580228-C-G

967779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25580303-A-G

http://identifiers.org/hco/9/GRCh38#967791-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#25580312-A-C

http://identifiers.org/hco/9/GRCh38#967894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#25580410-C-A

967894-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25580410-C-G

967894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25580410-C-T

967907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25580434-T-C

http://identifiers.org/hco/9/GRCh38#967928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#25580455-C-A

967928-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25580455-C-G

967928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25580455-C-T

967960-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25580526-C-G

967962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25580528-T-C

967962-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25580528-T-G

967966-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25580532-C-G

967966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: intron variant
orthologous variants: 25580532-C-T

968017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: synonymous variant
orthologous variants: 25580583-T-C

http://identifiers.org/hco/9/GRCh38#968052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#25580618-C-A

968155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: 3 prime UTR variant
orthologous variants: 25580721-G-A

968155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: 3 prime UTR variant
orthologous variants: 25580721-G-T

968170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: 3 prime UTR variant
orthologous variants: 25580743-G-A

968170-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: 3 prime UTR variant
orthologous variants: 25580743-G-C

http://identifiers.org/hco/9/GRCh38#968196-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#25580770-A-C

968196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: 3 prime UTR variant
orthologous variants: 25580770-A-G

968196-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: 3 prime UTR variant
orthologous variants: 25580770-A-T

968216-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: 3 prime UTR variant
orthologous variants: 25580789-G-C

968216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: 3 prime UTR variant
orthologous variants: 25580789-G-T

968406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: 3 prime UTR variant
orthologous variants: 25580992-T-C

968406-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: 3 prime UTR variant
orthologous variants: 25580992-T-G

http://identifiers.org/hco/9/GRCh38#968407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#25580993-C-A

968407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: 3 prime UTR variant
orthologous variants: 25580993-C-T

968580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: 3 prime UTR variant
orthologous variants: 25581162-C-T

968653-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: 3 prime UTR variant
orthologous variants: 25581230-T-G

968667-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: 3 prime UTR variant
orthologous variants: 25581248-G-C

968667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: 3 prime UTR variant
orthologous variants: 25581248-G-T

http://identifiers.org/hco/9/GRCh38#968680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#25581261-C-A

968759-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: 3 prime UTR variant
orthologous variants: 25581354-G-C

968759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: 3 prime UTR variant
orthologous variants: 25581354-G-T

968855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: 3 prime UTR variant
orthologous variants: 25581452-T-C

968863-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: 3 prime UTR variant
orthologous variants: 25581461-A-T

968864-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: 3 prime UTR variant
orthologous variants: 25581462-A-T

968883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: 3 prime UTR variant
orthologous variants: 25581483-C-T

968908-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: 3 prime UTR variant
orthologous variants: 25581508-G-C

968978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: 3 prime UTR variant
orthologous variants: 25581583-G-T

968979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: 3 prime UTR variant
orthologous variants: 25581584-G-A

968979-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: 3 prime UTR variant
orthologous variants: 25581584-G-C

968979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2934
most severe consequence: 3 prime UTR variant
orthologous variants: 25581584-G-T