5889730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 11782997-G-A

5889730-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 11782997-G-C

5889739-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: 5_prime_UTR_variant, splice_region_variant, undefined
orthologous variants: 11782988-C-G

http://identifiers.org/hco/10/GRCh38#5889823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#11782899-C-A

5889823-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 11782899-C-G

5889823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 11782899-C-T

http://identifiers.org/hco/10/GRCh38#5889849-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#11782846-A-C

5889849-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 11782846-A-T

http://identifiers.org/hco/10/GRCh38#5889864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#11782810-C-A

5889864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 11782810-C-T

5890012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, undefined
orthologous variants: 11782573-C-T

5890035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, undefined
orthologous variants: 11782550-G-T

http://identifiers.org/hco/10/GRCh38#5890080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#11782503-C-A

5890080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, undefined
orthologous variants: 11782503-C-T

http://identifiers.org/hco/10/GRCh38#5890094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#11782489-C-A

5890094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron variant
orthologous variants: 11782489-C-T

http://identifiers.org/hco/10/GRCh38#5890231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#11782352-C-A

5890231-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 11782352-C-G

5890231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 11782352-C-T

http://identifiers.org/hco/10/GRCh38#5890316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#11782271-C-A

5890316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11782271-C-T

5890330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11782257-G-A

5890330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11782257-G-T

5890551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 11782086-C-T

5890558-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 11782079-G-C

5890812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11781852-G-A

5890888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11781798-T-C

5890935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11781761-T-C

5890949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11781752-G-T

5891052-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11781634-G-C

5891077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11781605-G-T

5892060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11781227-C-T

http://identifiers.org/hco/10/GRCh38#5892062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#11781225-C-A

5892062-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11781225-C-G

5892205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11781111-G-A

5892399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11780939-T-C

5892670-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11780525-T-G

5892935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11780289-T-C

5893339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11780245-T-C

5893420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11780180-A-G

5893422-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11780178-C-G

5893627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11779997-A-G

5893843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11779790-G-A

5893843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11779790-G-T

5893990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11779639-C-T

5893991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11779638-G-A

5894128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11779207-C-T

5894161-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11779177-T-G

5894263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11779047-G-A

5894270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11779040-G-A

5894270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11779040-G-T

5894274-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11779036-T-A

5894274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11779036-T-C

5894478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11778539-G-A

http://identifiers.org/hco/10/GRCh38#5894481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#11778536-C-A

5894481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11778536-C-T

http://identifiers.org/hco/10/GRCh38#5895233-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#11777860-A-C

5895233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11777860-A-G

5895282-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11777832-G-C

5895282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11777832-G-T

5895327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11777790-G-A

5895405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11777708-G-A

5895564-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11777549-A-T

5895695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11777412-A-G

5895711-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11777395-A-T

5895840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11777241-C-T

5896011-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11777085-G-C

5900051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11776892-C-T

5900065-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11776874-C-G

5900065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11776874-C-T

5902953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11774803-G-A

5902953-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11774803-G-C

5902953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11774803-G-T

5902954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11774802-G-A

5902954-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11774802-G-C

5903005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11774752-G-A

5903005-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11774752-G-C

http://identifiers.org/hco/10/GRCh38#5903291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#11774481-C-A

5903291-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11774481-C-G

http://identifiers.org/hco/10/GRCh38#5905906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#11772647-C-A

5905906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11772647-C-T

5906141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11772416-G-T

http://identifiers.org/hco/10/GRCh38#5906148-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#11772409-A-C

5906148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11772409-A-G

5906207-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11772344-G-C

5906312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11772251-A-G

5906321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11772242-C-T

5906408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11772155-T-C

5906564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11771999-G-A

5906589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11771974-G-A

5907824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11769715-T-C

5908005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11769559-G-A

5908005-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11769559-G-C

5908171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11769454-T-C

5908270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11769357-T-C

5908491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11769203-A-G

5908597-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11769145-T-G

5908599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11769143-T-C

5909033-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11768934-C-G

5909033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11768934-C-T

5909195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11768778-T-C

5909356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11768611-G-T

http://identifiers.org/hco/10/GRCh38#5909598-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#11768421-A-C

5910894-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11767876-T-A

5910894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11767876-T-C

5910894-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11767876-T-G

5910909-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11767858-C-G

5910909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11767858-C-T

http://identifiers.org/hco/10/GRCh38#5911037-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#11767731-A-C

5911047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11767721-T-C

5911133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11767635-T-C

http://identifiers.org/hco/10/GRCh38#5911158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#11767614-C-A

5911158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11767614-C-T

5911263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11767571-A-G

5911279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11767555-A-G

5911436-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11767419-T-G

5911506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11767336-C-T

5911694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11767170-G-A

http://identifiers.org/hco/10/GRCh38#5911765-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#11767100-A-C

5911766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11767099-A-G

5911799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11767056-G-A

5911900-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11766976-T-G

5911940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11766934-C-T

5912801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11766198-C-T

5913277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11765838-G-A

5913531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11765600-A-G

5913535-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11765596-A-T

5913850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11765278-A-G

5913901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11765149-G-T

http://identifiers.org/hco/10/GRCh38#5913966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#11765042-C-A

5913966-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11765042-C-G

5913966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11765042-C-T

5914102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11764910-T-C

5914339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11764647-T-C

5914339-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11764647-T-G

5914422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11764582-G-A

5914805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11764261-G-A

5914871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11764202-C-T

5915238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11763413-A-G

5915245-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11763406-G-C

5915271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11763380-A-G

5915316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11763343-G-A

5915316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11763343-G-T

5915405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 11763255-A-G

5915405-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 11763255-A-T

http://identifiers.org/hco/10/GRCh38#5915531-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#11763129-A-C

5915531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11763129-A-G

http://identifiers.org/hco/10/GRCh38#5915616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#11763060-C-A

5915616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11763060-C-T

5915713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11762968-A-G

5915728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11762954-G-A

5915764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11762918-T-C

http://identifiers.org/hco/10/GRCh38#5915776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#11762908-C-A

5915776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11762908-C-T

5915792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11762889-G-T

http://identifiers.org/hco/10/GRCh38#5915978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#11762727-C-A

5915978-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron variant
orthologous variants: 11762727-C-G

5915978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron variant
orthologous variants: 11762727-C-T

5916035-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron variant
orthologous variants: 11762659-G-C

5916035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron variant
orthologous variants: 11762659-G-T

5916136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron variant
orthologous variants: 11762568-G-T

5916150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron variant
orthologous variants: 11762553-G-A

5916150-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron variant
orthologous variants: 11762553-G-C

5916150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron variant
orthologous variants: 11762553-G-T

5916285-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: synonymous variant
orthologous variants: 11762420-C-G

5916285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: synonymous variant
orthologous variants: 11762420-C-T

5916414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: synonymous variant
orthologous variants: 11762291-C-T

5916421-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: missense variant
orthologous variants: 11762284-G-C

5916465-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron variant
orthologous variants: 11762240-C-G

5916945-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron variant
orthologous variants: 11761873-T-A

5917074-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11761772-T-A

5917134-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11761750-T-A

5917136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11761748-A-G

5917234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11761672-A-G

5917279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11761639-G-A

5917279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11761639-G-T

5917317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11761602-G-A

5917361-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11761557-C-G

5917365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11761553-G-T

5917367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11761551-G-T

5917369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11761549-T-C

5917369-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11761549-T-G

5917693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron variant
orthologous variants: 11761209-G-A

5917722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron variant
orthologous variants: 11761180-A-G

5917723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron variant
orthologous variants: 11761179-G-T

5917725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron variant
orthologous variants: 11761177-G-A

5917725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron variant
orthologous variants: 11761177-G-T

5917813-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron variant
orthologous variants: 11761075-A-T

5917830-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron variant
orthologous variants: 11761057-C-G

5917858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron variant
orthologous variants: 11761027-C-T

5917863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron variant
orthologous variants: 11761022-G-A

5917915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron variant
orthologous variants: 11760974-G-A

5918081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron variant
orthologous variants: 11760828-T-C

5918216-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron variant
orthologous variants: 11760714-A-T

5918255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron variant
orthologous variants: 11760679-G-T

5918356-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: missense variant
orthologous variants: 11760572-G-C

5918503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron variant
orthologous variants: 11760406-G-A

5918503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron variant
orthologous variants: 11760406-G-T

5920843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron variant
orthologous variants: -T-C

5920843-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron variant
orthologous variants: -T-G

5921234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron variant
orthologous variants: 11756604-C-T

5921379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11756454-C-T

5921386-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11756448-G-C

5921404-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11756422-T-G

http://identifiers.org/hco/10/GRCh38#5921434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#11756393-C-A

5921477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11756352-G-A

5921522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11756307-G-A

5921585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11756244-T-C

5921592-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11756229-C-G

5921592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11756229-C-T

5921770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11755815-A-G

5921850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11755657-G-A

5921857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11755650-T-C

5922366-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11755160-A-T

http://identifiers.org/hco/10/GRCh38#5922428-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#11755101-A-C

5922713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11754868-G-A

5922713-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11754868-G-C

5922713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11754868-G-T

5922763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11754818-G-A

5923211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11754677-G-T

http://identifiers.org/hco/10/GRCh38#5923424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#11754522-C-A

5923424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11754522-C-T

5923708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11754328-C-T

http://identifiers.org/hco/10/GRCh38#5923732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#11754315-C-A

5923732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11754315-C-T

5923733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11754314-G-A

5923733-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11754314-G-C

5923812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11754272-A-G

5923813-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11754271-G-C

5923813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11754271-G-T

5923841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11754248-G-A

5923841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11754248-G-T

5923894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11754200-T-C

5924024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11754108-T-C

5924211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11753974-G-A

5924211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11753974-G-T

5924549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11753709-G-T

5924931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11753631-A-G

5925521-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11753136-C-G

5925521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11753136-C-T

5925582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11753092-A-G

5925585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11753089-G-T

5925706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11752987-C-T

5927170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11752241-G-A

5927316-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11752075-T-A

http://identifiers.org/hco/10/GRCh38#5927333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#11752060-C-A

5927333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11752060-C-T

5927493-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11751917-G-C

5927553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 11751857-G-A

5927627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11751786-G-A

5928513-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11751405-C-G

5928513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11751405-C-T

5928603-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11751319-C-G

5928643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11751275-G-A

5928720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11751177-G-A

5936220-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11748769-T-G

http://identifiers.org/hco/10/GRCh38#5936271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#11748714-C-A

5936271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11748714-C-T

5936284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11748707-T-C

5936415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11748605-A-G

5936621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11748405-A-G

5936666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11748359-G-A

5936680-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11748344-G-T

5936748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11748273-G-T

5936802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11748191-G-A

5936802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11748191-G-T

5936879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11748111-T-C

5936977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11747956-G-A

5936977-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11747956-G-C

5936977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11747956-G-T

http://identifiers.org/hco/10/GRCh38#5936978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#11747955-C-A

5936978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11747955-C-T

5937009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11747941-G-A

5937009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11747941-G-T

http://identifiers.org/hco/10/GRCh38#5937039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#11747910-C-A

5937039-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11747910-C-G

5937039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11747910-C-T

http://identifiers.org/hco/10/GRCh38#5937242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#11747710-C-A

5937242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 11747710-C-T

5937272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11747680-G-A

5937272-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11747680-G-C

5937335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11747652-A-G

5937408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11747577-C-T

http://identifiers.org/hco/10/GRCh38#5937426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#11747559-C-A

5937426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11747559-C-T

5937427-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11747558-T-A

5937427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11747558-T-C

http://identifiers.org/hco/10/GRCh38#5937463-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#11747522-A-C

5937463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11747522-A-G

5937489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11747496-G-A

5937489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13620
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11747496-G-T