103109569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 7176961-C-T

103109728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 7176802-A-G

103109736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 7176794-G-A

103109776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant, undefined
orthologous variants: 7176734-T-C

103109776-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant, undefined
orthologous variants: 7176734-T-G

103112610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7176344-A-G

103112810-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7176200-T-G

103113314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7175633-T-C

103113550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 7175397-A-G

http://identifiers.org/hco/11/GRCh38#103113673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7175274-C-A

103113673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 7175274-C-T

103113711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7175236-A-G

103113713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7175234-A-G

103113776-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7175183-A-T

103115322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7172774-T-C

103115322-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7172774-T-G

103115336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7172760-A-G

103115516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7172536-G-A

103115516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7172536-G-T

103116086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7172011-T-C

103116178-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7171690-G-C

103116362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7171470-A-G

103116538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7171034-T-C

103116646-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 7170928-A-T

103116748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7170828-A-G

103116750-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7170826-A-T

http://identifiers.org/hco/11/GRCh38#103116752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7170755-C-A

103116754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7170753-T-C

103116754-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7170753-T-G

103117362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7169972-T-C

103117407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7169903-A-G

103117560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7169764-G-A

103117663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 7169675-T-C

103117747-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 7169591-G-C

103117792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 7169546-G-A

103117792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 7169546-G-T

103117812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 7169526-T-C

103117855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 7169483-C-T

103117880-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7169458-C-G

http://identifiers.org/hco/11/GRCh38#103117916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7169423-C-A

103117936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7169403-A-G

103118041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7169256-G-A

103118185-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7169116-G-C

103118188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7169113-T-C

103118256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7169049-T-C

http://identifiers.org/hco/11/GRCh38#103120368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7168889-C-A

103120368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7168889-C-T

103120412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7168845-T-C

103120591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7168666-A-G

103120612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7168647-G-A

103120612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7168647-G-T

103120641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7168618-A-G

103120641-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7168618-A-T

103120672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7168587-G-A

103120681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 7168578-G-A

103120681-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 7168578-G-C

103120681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 7168578-G-T

103120707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 7168552-G-A

http://identifiers.org/hco/11/GRCh38#103120734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7168525-C-A

103120734-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 7168525-C-G

103120734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 7168525-C-T

103120892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7168392-G-A

103121050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7168237-A-G

103121050-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7168237-A-T

103121088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7168200-T-C

103121094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7168194-T-C

103121108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7168182-A-G

http://identifiers.org/hco/11/GRCh38#103121109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7168181-C-A

103121109-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7168181-C-G

103121123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7168166-A-G

103121154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7168144-G-T

103121559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7167052-G-T

103121564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7167048-T-C

http://identifiers.org/hco/11/GRCh38#103121574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7167038-C-A

http://identifiers.org/hco/11/GRCh38#103121950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7166511-C-A

103121950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7166511-C-T

103122487-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7166089-A-T

103122609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7165990-G-A

103122642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7165956-T-C

103122682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7165916-C-T

103122705-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7165894-T-A

http://identifiers.org/hco/11/GRCh38#103122739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7165861-C-A

103122739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7165861-C-T

103122852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 7165745-G-A

103122852-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 7165745-G-C

103122852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 7165745-G-T

http://identifiers.org/hco/11/GRCh38#103122933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7165664-C-A

103122963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 7165634-A-G

103122963-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 7165634-A-T

http://identifiers.org/hco/11/GRCh38#103123640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7164442-C-A

103123648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7164434-A-G

103123808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7164291-G-A

103124042-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7164074-T-G

103124095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7164022-G-A

103128374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7160723-G-A

103128670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7160467-C-T

103128822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7160322-A-G

http://identifiers.org/hco/11/GRCh38#103128876-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7160272-A-C

103129215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7159989-C-T

103129304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7159896-T-C

103133523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7159659-A-G

103133561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 7159625-A-G

103133947-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7159240-T-G

103134192-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7159038-T-A

103134192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7159038-T-C

103134192-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7159038-T-G

103134198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7159032-G-A

103134198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7159032-G-T

103134199-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7159031-T-A

103134199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7159031-T-C

103134199-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7159031-T-G

103134300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7158944-G-A

103134300-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7158944-G-C

103134300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7158944-G-T

http://identifiers.org/hco/11/GRCh38#103134301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7158943-C-A

103134301-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7158943-C-G

103134301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7158943-C-T

http://identifiers.org/hco/11/GRCh38#103134736-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7158658-C-A

103134736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7158658-C-T

103135043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7158436-T-C

103135227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7158288-A-G

103135428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7158092-A-G

103136078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7157447-G-A

103136078-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7157447-G-C

103142892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7155434-G-A

103142901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7155425-A-G

http://identifiers.org/hco/11/GRCh38#103143499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7154846-C-A

103143499-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7154846-C-G

103143625-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7154722-A-T

103143856-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7154497-G-C

103143923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7154432-T-C

103144015-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7154358-T-A

103144272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7151739-A-G

103144436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7151588-A-G

103144450-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7151573-T-A

103147843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 7148667-A-G

103147898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7148614-A-G

103147949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7148564-T-C

103147953-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7148560-T-A

103148259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7148059-C-T

103148398-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7147912-T-G

103148448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7147848-G-T

103148627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7147672-A-G

http://identifiers.org/hco/11/GRCh38#103148628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7147671-C-A

103148628-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7147671-C-G

103152081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7145736-G-A

103152081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7145736-G-T

103152100-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7145718-T-A

103152157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 7145675-G-A

103152157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 7145675-G-T

http://identifiers.org/hco/11/GRCh38#103152161-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7145671-A-C

103152161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 7145671-A-G

103152190-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 7145642-G-C

103152190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 7145642-G-T

103152292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 7145540-A-G

103153109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7144485-A-G

http://identifiers.org/hco/11/GRCh38#103153250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7144386-C-A

103153250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7144386-C-T

103153293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7144351-T-C

103153532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7144119-T-C

103153561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7144091-T-C

103153640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7144006-A-G

103154264-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7143124-A-T

103154427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7143034-A-G

103154446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 7143015-T-C

103154446-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 7143015-T-G

http://identifiers.org/hco/11/GRCh38#103154532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7142929-C-A

103154532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 7142929-C-T

103154684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 7142773-G-A

103154684-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 7142773-G-C

103154728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 7142729-G-A

103154728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 7142729-G-T

103155234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7142460-G-A

103155234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7142460-G-T

103155281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7142420-A-G

103155281-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7142420-A-T

103155331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, splice_region_variant
orthologous variants: 7142368-A-G

103155331-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, splice_region_variant
orthologous variants: 7142368-A-T

103155364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 7142335-G-A

103155364-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 7142335-G-C

103155481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 7142218-G-T

103155493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 7142206-G-A

103155512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 7142185-C-T

103155600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 7141998-G-A

103155612-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 7141984-T-A

103155693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 7141902-G-A

103156424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 7141243-A-G

103157935-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7139912-T-G

103158612-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7139558-A-T

103158635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7139546-A-G

103158635-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7139546-A-T

103158650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7139531-G-A

103158650-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7139531-G-C

103158650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7139531-G-T

http://identifiers.org/hco/11/GRCh38#103158756-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7139425-A-C

103158756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 7139425-A-G

103158780-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 7139401-T-A

103158780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 7139401-T-C

103158973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 7139213-G-A

103159171-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7139039-T-G

103159244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7138988-G-A

103159893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7138433-G-A

103159929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7138397-A-G

103160067-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7138253-T-G

103160079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7138242-A-G

103160398-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7137774-T-G

103160659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7137491-C-T

103160685-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7137478-T-A

103160686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7137477-G-A

103160775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7137399-A-G

103160840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7137284-T-C

103160848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7137276-A-G

http://identifiers.org/hco/11/GRCh38#103160904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7137174-C-A

103160904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7137174-C-T

103160952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 7137088-G-T

http://identifiers.org/hco/11/GRCh38#103161027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7137013-C-A

103161027-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 7137013-C-G

103161072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7136978-A-G

103161123-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7136949-T-G

103161334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7136733-T-C

http://identifiers.org/hco/11/GRCh38#103161680-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7136616-A-C

103161680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7136616-A-G

103161821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7136541-G-A

http://identifiers.org/hco/11/GRCh38#103162075-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7136364-A-C

103162080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7136359-T-C

103162485-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7135579-T-G

103162906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7135223-A-G

103162930-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7135200-T-G

103163190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7134984-G-A

103166002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 7134288-G-A

103166045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 7134245-A-G

103166100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7134017-T-C

103166223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7133833-A-G

103166264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7133794-C-T

103166381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7133706-G-A

103168625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7132143-T-C

103168681-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7132095-T-A

103169002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7131791-A-G

103170058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7130920-A-G

http://identifiers.org/hco/11/GRCh38#103170073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7130909-C-A

103170073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7130909-C-T

103170103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 7130879-T-C

103170417-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7130463-A-T

103170875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7129854-T-C

http://identifiers.org/hco/11/GRCh38#103170898-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7129831-A-C

103170898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 7129831-A-G

103170982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 7129747-G-A

103170991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 7129738-G-T

103171045-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 7129684-G-C

http://identifiers.org/hco/11/GRCh38#103172852-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7129330-A-C

103173010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7129203-A-G

103173199-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 7129060-T-A

103173567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7128723-A-G

103173769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7128537-A-G

103174172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, splice_donor_variant
orthologous variants: 7128154-T-C

103174174-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7128152-T-A

103174174-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7128152-T-G

103174202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7128125-A-G

103174202-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7128125-A-T

103174214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7128113-A-G

103174698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7127590-A-G

103175032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7127309-A-G

103175083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7127266-T-C

103175565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7126696-A-G

103175611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7126651-G-A

103175642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7126620-T-C

103175890-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7126236-A-T

http://identifiers.org/hco/11/GRCh38#103176159-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7126002-A-C

103176159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7126002-A-G

103176291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 7125872-A-G

103176369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 7125794-G-T

103176576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7125606-T-C

103177157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7125319-A-G

103177413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7125109-G-A

103177413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7125109-G-T

103177483-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7125048-T-A

103177483-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7125048-T-G

103177539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7125011-T-C

103177622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 7124928-A-G

103177730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, stop_gained
orthologous variants: 7124820-C-T

http://identifiers.org/hco/11/GRCh38#103177787-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7124763-A-C

103177847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7124717-T-C

103178035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7124519-A-G

103178687-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7123787-T-A

http://identifiers.org/hco/11/GRCh38#103178889-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7123032-C-A

103178889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7123032-C-T

http://identifiers.org/hco/11/GRCh38#103178890-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7123031-A-C

103178890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7123031-A-G

103178890-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7123031-A-T

103178946-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7122915-G-C

103178946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7122915-G-T

103179003-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7122836-C-G

103179193-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 7122646-T-A

103179193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 7122646-T-C

103179380-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7122273-T-G

103179490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7122184-G-A

103179490-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7122184-G-C

103180011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7121665-T-C

103180170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7121527-A-G

103180170-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7121527-A-T

103181649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7121033-G-A

103181649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7121033-G-T

103181750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 7120943-G-T

103182046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7120656-G-A

103182360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7120506-A-G

103183015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7119906-T-C

103183160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7119773-A-G

103183332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7119639-A-G

103184673-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7119199-T-A

103184786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7119088-A-G

103184814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7119060-G-A

103184814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7119060-G-T

103184828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7119052-G-A

103184839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7119041-T-C

103184968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 7118912-G-A

103184968-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 7118912-G-C

103185089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7118789-T-C

103185197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7118669-G-A

103185197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7118669-G-T

103185654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7118102-C-T

103185670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7118086-G-T

103185872-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7117965-G-C

103186175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7117697-G-A

103186175-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7117697-G-C

103186175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7117697-G-T

103186577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7117347-A-G

103186577-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7117347-A-T

103186617-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7117309-A-T

http://identifiers.org/hco/11/GRCh38#103186654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7117270-C-A

103187163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7116854-T-C

http://identifiers.org/hco/11/GRCh38#103187189-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7116824-A-C

103187189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7116824-A-G

103187189-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7116824-A-T

103187193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7116820-A-G

103187404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 7116574-G-A

103187404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 7116574-G-T

103187621-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7116357-T-G

103187622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7116356-G-A

103187634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7116355-A-G

103187668-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7116328-T-A

103187668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7116328-T-C

103188188-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7115667-T-G

103188208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7115647-T-C

103188260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7115598-G-A

103188356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7115509-G-A

103188356-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7115509-G-C

103188356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7115509-G-T

http://identifiers.org/hco/11/GRCh38#103188360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7115508-C-A

103188360-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7115508-C-G

103188360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7115508-C-T

http://identifiers.org/hco/11/GRCh38#103188642-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7114869-C-A

103188642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 7114869-C-T

103188803-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7114742-G-C

103188838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7114719-G-A

103188871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7114699-A-G

http://identifiers.org/hco/11/GRCh38#103188969-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7113907-A-C

103188998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7113879-A-G

103189410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7113499-G-T

http://identifiers.org/hco/11/GRCh38#103189536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7113367-C-A

103189536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7113367-C-T

103189790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 7113110-G-A

103189790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, stop_gained
orthologous variants: 7113110-G-T

103189821-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7113079-A-T

103190800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7112641-G-A

103190940-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7112545-G-C

103190940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7112545-G-T

http://identifiers.org/hco/11/GRCh38#103191439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7112228-C-A

http://identifiers.org/hco/11/GRCh38#103191464-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7112204-A-C

103191464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7112204-A-G

http://identifiers.org/hco/11/GRCh38#103191482-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7112196-A-C

103191482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7112196-A-G

103191494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7112171-G-A

103191494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7112171-G-T

103191517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, splice_region_variant
orthologous variants: 7112148-G-A

103191517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, splice_region_variant
orthologous variants: 7112148-G-T

103191541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 7112124-G-A

103191607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 7112058-G-A

103191607-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 7112058-G-C

103191607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 7112058-G-T

103191706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7111952-G-A

103191706-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7111952-G-C

103191732-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7111929-T-A

http://identifiers.org/hco/11/GRCh38#103191970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7111728-C-A

103191970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7111728-C-T

103192287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7111400-A-G

103192333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7111354-G-A

103192333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7111354-G-T

103192427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7111260-G-A

103192427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7111260-G-T

http://identifiers.org/hco/11/GRCh38#103192881-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7110690-A-C

103193119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7110543-G-A

103193417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7110272-G-A

http://identifiers.org/hco/11/GRCh38#103197881-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7103824-A-C

103197881-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7103824-A-T

103198180-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7103541-T-G

103198369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7103371-T-C

103199923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7101944-T-C

103199938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7101926-A-G

http://identifiers.org/hco/11/GRCh38#103199958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7101879-C-A

http://identifiers.org/hco/11/GRCh38#103199967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7101767-C-A

103199981-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7101741-A-T

103200035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7101609-T-C

http://identifiers.org/hco/11/GRCh38#103200164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7101480-C-A

103200164-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7101480-C-G

103200164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7101480-C-T

103200194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7101452-G-A

http://identifiers.org/hco/11/GRCh38#103200229-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7101417-A-C

http://identifiers.org/hco/11/GRCh38#103203638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7101214-C-A

103203782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7101066-T-C

103203874-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7085826-T-G

103204303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7085754-G-A

103204365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7085693-G-A

103204644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7085441-A-G

http://identifiers.org/hco/11/GRCh38#103204690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7085246-C-A

103204724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7085212-A-G

http://identifiers.org/hco/11/GRCh38#103204729-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7085207-C-A

http://identifiers.org/hco/11/GRCh38#103204920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7084976-C-A

103204920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 7084976-C-T

103204959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 7084937-A-G

103205085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7084813-T-C

103205085-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7084813-T-G

103205109-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7084786-T-A

103209936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 7083179-A-G

103210171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7082966-A-G

103210537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7082373-T-C

103210748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7082185-G-A

http://identifiers.org/hco/11/GRCh38#103210781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7082147-C-A

103210800-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7082128-A-T

103210902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7082054-G-A

103210904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7082052-G-T

http://identifiers.org/hco/11/GRCh38#103211023-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7081908-A-C

103211102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7081840-A-G

103211116-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7081827-T-A

103211128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7081815-A-G

103211143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7081800-C-T

103211195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7081754-G-T

103211684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7081235-A-G

103211724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7081218-A-G

http://identifiers.org/hco/11/GRCh38#103211775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7081170-C-A

103211775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7081170-C-T

103211956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7080989-T-C

103212041-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7080877-T-A

103212288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7080672-G-A

103212288-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7080672-G-C

103212454-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7080553-T-G

103212710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7080294-G-A

103212804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7079300-C-T

103213173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7078974-G-A

103215636-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7078088-T-G

http://identifiers.org/hco/11/GRCh38#103215655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7078069-C-A

103215655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7078069-C-T

103215771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 7077957-C-T

103215800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 7077928-T-C

103216011-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron variant
orthologous variants: 7077726-G-C

103216011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron variant
orthologous variants: 7077726-G-T

http://identifiers.org/hco/11/GRCh38#103219875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7076365-C-A

http://identifiers.org/hco/11/GRCh38#103220073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7076150-C-A

103220073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron variant
orthologous variants: 7076150-C-T

103220305-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron variant
orthologous variants: 7076046-A-T

103220665-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, missense_variant
orthologous variants: 7075878-C-G

103220665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, missense_variant
orthologous variants: 7075878-C-T

103220692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 7075851-C-T

103220710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, missense_variant
orthologous variants: 7075833-G-A

103220843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron variant
orthologous variants: 7072774-G-T

103220924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron variant
orthologous variants: 7072694-G-A

103220924-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron variant
orthologous variants: 7072694-G-T

103221245-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron variant
orthologous variants: 7072363-T-A

103221261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron variant
orthologous variants: 7072347-C-T

103221313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron variant
orthologous variants: 7072311-T-C

103221963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron variant
orthologous variants: 7071988-A-G

103221982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron variant
orthologous variants: 7071969-C-T

103222159-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron variant
orthologous variants: 7071788-T-G

103222219-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron variant
orthologous variants: 7071763-T-A

103222219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron variant
orthologous variants: 7071763-T-C

103222219-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron variant
orthologous variants: 7071763-T-G

http://identifiers.org/hco/11/GRCh38#103222266-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7071712-A-C

103222266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron variant
orthologous variants: 7071712-A-G

103222266-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron variant
orthologous variants: 7071712-A-T

103222501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron variant
orthologous variants: 7071539-T-C

103223106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron variant
orthologous variants: 7070986-T-C

103231178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron variant
orthologous variants: 7052716-G-A

103231178-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron variant
orthologous variants: 7052716-G-T

103231282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, missense_variant
orthologous variants: 7052623-A-G

103233560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron variant
orthologous variants: 7051894-G-A

http://identifiers.org/hco/11/GRCh38#103234201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7051342-C-A

103234201-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron variant
orthologous variants: 7051342-C-G

103234201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron variant
orthologous variants: 7051342-C-T

103235907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron variant
orthologous variants: 7050292-T-C

103236017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron variant
orthologous variants: 7050181-A-G

103236338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron variant
orthologous variants: 7049261-G-A

103236338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron variant
orthologous variants: 7049261-G-T

103236339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron variant
orthologous variants: 7049260-G-T

103237047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron variant
orthologous variants: 7048655-T-C

103237307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron variant
orthologous variants: 7048113-A-G

103237730-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron variant
orthologous variants: 7047615-T-A

103237893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron variant
orthologous variants: 7047361-A-G

103238062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron variant
orthologous variants: 7047228-C-T

103238127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron variant
orthologous variants: 7047165-G-A

103238127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron variant
orthologous variants: 7047165-G-T

103240412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron variant
orthologous variants: 7046725-G-A

103240520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron variant
orthologous variants: 7046290-G-A

103240777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron variant
orthologous variants: 7046057-T-C

103241203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron variant
orthologous variants: 7045674-G-T

103241226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron variant
orthologous variants: 7045652-G-A

103241395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron variant
orthologous variants: 7045491-T-C

103241462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron variant
orthologous variants: 7045431-G-T

103241577-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron variant
orthologous variants: 7045317-T-A

103241713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron variant
orthologous variants: 7045192-G-A

103243476-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron variant
orthologous variants: 7044619-A-T

103243897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron variant
orthologous variants: 7044228-G-A

103243897-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron variant
orthologous variants: 7044228-G-C

103243917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron variant
orthologous variants: 7044200-G-T

http://identifiers.org/hco/11/GRCh38#103245302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7041672-C-A

103245302-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, missense_variant
orthologous variants: 7041672-C-G

103245302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, missense_variant
orthologous variants: 7041672-C-T

103245320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, missense_variant
orthologous variants: 7041654-G-A

103245320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, missense_variant
orthologous variants: 7041654-G-T

103245365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, missense_variant
orthologous variants: 7041609-G-A

103245365-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, missense_variant
orthologous variants: 7041609-G-C

103245365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, missense_variant
orthologous variants: 7041609-G-T

103245468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron variant
orthologous variants: 7041513-G-T

103245476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron variant
orthologous variants: 7041505-A-G

103245766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron variant
orthologous variants: 7041181-A-G

103252610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7038805-G-A

103252610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7038805-G-T

103252975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7038286-A-G

http://identifiers.org/hco/11/GRCh38#103253182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7037912-C-A

103253182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7037912-C-T

103253203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7037891-T-C

103253437-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 7037662-T-G

103253593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7037521-G-A

103253593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7037521-G-T

103253761-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7037395-G-C

103253780-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7037374-A-T

103254013-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7037044-T-A

103254244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7036831-T-C

103254383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7036695-A-G

103254396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7036687-A-G

103255142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7035974-A-G

103255564-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7035575-T-A

103255564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7035575-T-C

103255859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7035271-G-A

http://identifiers.org/hco/11/GRCh38#103255992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7035215-C-A

103255992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7035215-C-T

103256076-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7035151-T-A

103256076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7035151-T-C

http://identifiers.org/hco/11/GRCh38#103256266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7034962-C-A

103256266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7034962-C-T

103256267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7034961-G-A

103256268-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7034960-T-A

103256276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7034952-T-C

103256284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7034944-A-G

103256299-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7034929-T-A

103256299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7034929-T-C

103256307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7034921-A-G

http://identifiers.org/hco/11/GRCh38#103256308-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7034920-A-C

103256308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7034920-A-G

103256308-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7034920-A-T

103256347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7034882-G-A

103256347-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7034882-G-C

103256353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7034876-A-G

103256362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7034867-A-G

103256362-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7034867-A-T

103256384-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7034845-G-C

103256384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7034845-G-T

103256674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7032635-T-C

103257375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7031964-G-T

103257500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7031871-G-A

103257500-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7031871-G-C

103257500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7031871-G-T

103257504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7031867-T-C

103257533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7031855-T-C

103257538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7031850-T-C

103257560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7031828-A-G

103257737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 7031653-C-T

http://identifiers.org/hco/11/GRCh38#103257775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7031629-C-A

103257775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7031629-C-T

103257897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7031513-A-G

103258144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7031299-G-A

103258156-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7031287-C-G

103259718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7023753-T-C

103259797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7023681-A-G

103259797-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7023681-A-T

103259873-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7023413-A-T

103259996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7023295-T-C

103259996-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7023295-T-G

103260032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7023256-G-A

103260032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7023256-G-T

103260035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7023253-A-G

103260073-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7023225-A-T

http://identifiers.org/hco/11/GRCh38#103260111-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7023175-A-C

103260112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7023174-T-C

103260219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7023064-G-T

103260224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7023059-C-T

103260287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7022994-A-G

103260287-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7022994-A-T

103260376-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7022894-G-C

103267389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7022065-A-G

103267479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7021974-G-A

103267832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7021588-A-G

103267937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7021484-T-C

103267977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7021450-A-G

103268051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7021355-T-C

103268700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7020780-A-G

103269217-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7020276-G-C

103269239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7020256-G-A

103269306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7020190-T-C

103269323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7020174-G-T

103269607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7019969-G-A

103269694-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7019883-A-T

103270972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7019150-G-T

103271521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7018263-G-A

103271722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7018094-G-A

103272740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7017899-G-A

103272747-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7017892-T-G

103273785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7017331-C-T

103273874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7017267-C-T

103273918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7017237-A-G

103273990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7017162-G-A

103280328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7016816-A-G

103280384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 7016757-G-A

103280384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 7016757-G-T

103280432-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7016709-G-C

103280432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7016709-G-T

103280481-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7016661-T-G

103280815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7016327-A-G

103280817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7016325-A-G

103280840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7016302-C-T

103280953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7016212-G-A

103280953-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7016212-G-C

103282094-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7015607-A-T

103282114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7015587-T-C

103282154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7015547-G-A

103282154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7015547-G-T

http://identifiers.org/hco/11/GRCh38#103282710-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7014507-A-C

103282908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7014326-A-G

103282967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7014261-T-C

103282997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7014225-T-C

http://identifiers.org/hco/11/GRCh38#103283091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7014129-C-A

103283091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7014129-C-T

103283511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7013362-C-T

103283639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7013242-A-G

103283665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7013216-T-C

103283891-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7013064-A-T

103283901-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7013054-T-G

http://identifiers.org/hco/11/GRCh38#103284484-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7012511-A-C

103284484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7012511-A-G

103284527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7012402-A-G

103284662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7012258-A-G

103286071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7011460-C-T

103286076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7011455-A-G

103286125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7011413-A-G

103286413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7011144-A-G

103286496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7011057-G-A

103286496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7011057-G-T

103286595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7010966-A-G

103286630-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7010933-A-T

103286721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7010836-A-G

103286737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7010820-G-A

103287004-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7010610-A-T

103287298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7010256-C-T

103287404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7010157-A-G

103287443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7010120-A-G

103287467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7010102-T-C

103287651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7009925-T-C

103287710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7009868-C-T

103303061-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7006907-T-A

103303081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7006886-T-C

103303176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 7006791-A-G

103303266-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7006701-T-A

http://identifiers.org/hco/11/GRCh38#103303269-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7006699-C-A

103303269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7006699-C-T

http://identifiers.org/hco/11/GRCh38#103303698-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7006419-A-C

103303698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7006419-A-G

103303839-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7006305-T-A

103304054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7006095-A-G

103304233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7005949-G-A

103304265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7005922-A-G

103304287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7005901-T-C

103304296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7005897-G-A

103304304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7005889-T-C

103304451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7005752-G-T

103304459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7005742-T-C

103304459-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7005742-T-G

103304492-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7005709-G-C

103304492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7005709-G-T

103304787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7005078-G-A

103304787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7005078-G-T

103304966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7004892-G-A

103305018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7004821-C-T

103305288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7004552-T-C

http://identifiers.org/hco/11/GRCh38#103305536-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7004362-A-C

103305580-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7004316-A-T

103306321-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7003911-T-G

103306579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7003704-A-G

103306722-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7003571-T-A

http://identifiers.org/hco/11/GRCh38#103307047-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7003238-A-C

103307047-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7003238-A-T

103307262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7003080-A-G

103307432-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7002927-A-T

103307851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7002535-G-A

103307851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7002535-G-T

103307968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7002431-G-A

103307968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7002431-G-T

103307971-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7002428-T-A

103307971-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7002428-T-G

103307973-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7002426-A-T

103311456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7001897-T-C

103311663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7001702-T-C

103311770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7001603-G-A

http://identifiers.org/hco/11/GRCh38#103311848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#7001528-C-A

103312047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7001325-T-C

103312047-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7001325-T-G

103312057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7001309-A-G

103315916-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6997474-C-G

103316015-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6997369-T-G

103316272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6997154-A-G

103316425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6997040-T-C

103316449-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6997028-G-T

103316463-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6997008-T-G

http://identifiers.org/hco/11/GRCh38#103316476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6996994-C-A

103316476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6996994-C-T

103316489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6996981-A-G

103316507-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6996963-T-G

103316538-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 6996944-T-A

103316538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 6996944-T-C

103316545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, splice_region_variant
orthologous variants: 6996937-G-A

103316545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, splice_region_variant
orthologous variants: 6996937-G-T

103316673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6996844-G-A

103316673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6996844-G-T

103316684-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6996833-T-A

103316684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6996833-T-C

103316698-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6996815-A-T

103316755-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6996754-T-A

103316957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6996520-G-T

http://identifiers.org/hco/11/GRCh38#103317215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6996338-C-A

103317230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6996325-A-G

103318034-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6995884-C-G

http://identifiers.org/hco/11/GRCh38#103319631-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6995694-A-C

103319866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6995487-G-A

103319883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6995467-G-A

103319945-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6995403-T-A

103319971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6995377-C-T

103320522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6994999-A-G

103320667-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6994801-T-G

103320887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6994445-A-G

103321199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 6993974-C-T

http://identifiers.org/hco/11/GRCh38#103322362-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6993836-A-C

103322450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6993762-A-G

103322495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6993717-G-A

103322824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6993501-A-G

103322996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6993377-C-T

103323367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6993041-C-T

http://identifiers.org/hco/11/GRCh38#103323716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6992733-C-A

103323892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 6992620-C-T

103323985-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 6992527-T-G

103346652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6988850-T-C

103346913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6988634-G-A

103346940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6988606-G-A

http://identifiers.org/hco/11/GRCh38#103346971-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6988579-A-C

103347104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6988454-A-G

103347203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6988386-A-G

103347370-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6988225-T-G

103347856-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6987881-A-T

103347911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6987848-G-A

103348082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6987722-G-A

103348082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6987722-G-T

103348213-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6987316-C-G

103348464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6987077-T-C

http://identifiers.org/hco/11/GRCh38#103349458-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6986027-A-C

103349649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6985822-G-A

103349649-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6985822-G-C

http://identifiers.org/hco/11/GRCh38#103349776-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6985701-A-C

103349776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6985701-A-G

103349796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6985681-C-T

103356392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6985280-G-A

103356430-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6985244-G-C

103356476-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6985201-A-T

103356840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6984838-T-C

103356942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6984742-G-A

103357034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6984648-C-T

103357214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6984137-G-T

103357391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6983958-G-A

103357391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6983958-G-T

103357429-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6983926-A-T

103358167-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6983579-T-G

103358215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6983530-T-C

103358227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6983518-T-C

103358243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, splice_region_variant
orthologous variants: 6983504-G-A

103358243-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, splice_region_variant
orthologous variants: 6983504-G-C

103358243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, splice_region_variant
orthologous variants: 6983504-G-T

103358273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 6983474-T-C

103358282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 6983465-G-A

103358282-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 6983465-G-C

103358282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 6983465-G-T

http://identifiers.org/hco/11/GRCh38#103358321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6983426-C-A

103358321-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 6983426-C-G

103358321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 6983426-C-T

103358504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6983142-A-G

103358524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6983122-T-C

103358546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6983102-T-C

103364177-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6982984-G-C

103364229-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6982966-T-A

103364238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6982957-A-G

103366515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6982442-G-A

103366515-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6982442-G-C

103366560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6982391-C-T

103366610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6982353-C-T

103366672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6982295-C-T

103366836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6982150-A-G

103367095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6981904-G-T

103367124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6981877-A-G

103378609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6981308-G-A

103378631-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6981286-C-G

103378631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6981286-C-T

103378906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6981016-A-G

103379090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6980835-T-C

103379242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6980452-A-G

103379255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6980439-C-T

103379450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6980228-T-C

103379512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6980046-A-G

http://identifiers.org/hco/11/GRCh38#103379850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6979738-C-A

103379957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6971034-A-G

103379957-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6971034-A-T

103380889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6970678-G-A

103381835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6970217-A-G

103382351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6969697-C-T

103399526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6967407-A-G

103399527-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6967406-C-G

103399562-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6967385-T-A

103399562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6967385-T-C

103399879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 6967071-G-A

103399879-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 6967071-G-C

103399908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6967058-T-C

http://identifiers.org/hco/11/GRCh38#103399932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6967034-C-A

103399981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6966983-A-G

103399996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6966969-A-G

103400003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6966962-A-G

103400095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6966872-T-C

103400095-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6966872-T-G

103400216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6966743-G-A

103400562-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6966578-C-G

http://identifiers.org/hco/11/GRCh38#103435635-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6956181-A-C

103435973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 6955964-G-T

103435985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 6955952-C-T

103436037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6955900-G-A

103436037-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6955900-G-C

103436114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6955837-G-A

103436114-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6955837-G-C

103436148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6955825-T-C

103436889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6955334-C-T

103437203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6955150-C-T

103437206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6955147-G-A

103437247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6955102-G-A

103437355-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6954993-G-C

103437366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6954978-G-A

103437369-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6954975-C-G

103437611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6954773-A-G

103437673-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6954727-G-C

103437721-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6954701-T-G

103438183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6954493-T-C

103438186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6954490-A-G

103438242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6954436-C-T

103438570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6954174-T-C

103438615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6954131-G-A

103438647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6954098-G-A

103438831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6953928-T-C

http://identifiers.org/hco/11/GRCh38#103452919-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6944299-A-C

103452934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6944279-A-G

103453037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6944171-C-T

103453052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6944157-G-A

103453053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6944156-T-C

103453262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6943941-A-G

103453380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6943813-C-T

103453445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6943756-A-G

103453670-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6943525-T-G

103454172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6942592-C-T

103454341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6942435-A-G

103454451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6942338-G-A

http://identifiers.org/hco/11/GRCh38#103454660-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6942176-A-C

103454897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6941959-A-G

http://identifiers.org/hco/11/GRCh38#103454907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6941949-C-A

103454907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6941949-C-T

103454932-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6941924-T-G

103454935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6941923-G-A

103454935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6941923-G-T

http://identifiers.org/hco/11/GRCh38#103454962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6941896-C-A

103454962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6941896-C-T

103455059-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6941813-A-T

103455103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6941770-A-G

103455103-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6941770-A-T

103455106-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6941767-T-A

103455106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6941767-T-C

103455142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6941748-A-G

103455323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6941571-T-C

http://identifiers.org/hco/11/GRCh38#103455333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6941563-C-A

103455333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6941563-C-T

103455379-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6941518-T-A

103455379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6941518-T-C

103455657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6941271-A-G

103455807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6941126-C-T

103456018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6940976-A-G

103456212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6940775-T-C

103456238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6940658-A-G

http://identifiers.org/hco/11/GRCh38#103456390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6940512-C-A

103456390-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6940512-C-G

103456390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6940512-C-T

http://identifiers.org/hco/11/GRCh38#103456391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6940511-C-A

103456438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6940472-G-T

103456510-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6940411-G-C

103468263-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6935631-T-A

103468288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6935608-C-T

http://identifiers.org/hco/11/GRCh38#103468390-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6935535-A-C

http://identifiers.org/hco/11/GRCh38#103468419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6935506-C-A

103468551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6935390-T-C

103468667-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6935275-T-A

103468709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6935233-A-G

103468709-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6935233-A-T

http://identifiers.org/hco/11/GRCh38#103468721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6935227-C-A

103468721-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6935227-C-G

103468803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6935146-G-A

103468803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6935146-G-T

http://identifiers.org/hco/11/GRCh38#103468838-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6935111-A-C

103474929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6931054-C-T

103474970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6931011-A-G

103475446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6930585-G-A

103478966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6929735-T-C

103478994-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6929701-T-G

103479009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6929682-T-C

103479009-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6929682-T-G

103479055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6929663-G-A

103479055-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6929663-G-C

http://identifiers.org/hco/11/GRCh38#103479146-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6929570-A-C

103479146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6929570-A-G

103479254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 6929462-A-G

103479272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 6929446-G-A

103479272-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 6929446-G-C

103479290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 6929429-A-G

http://identifiers.org/hco/11/GRCh38#103479307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6929414-C-A

103479401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 6929307-G-A

http://identifiers.org/hco/11/GRCh38#103479504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6929219-C-A

103479504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 6929219-C-T

103479541-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 6929194-A-T

http://identifiers.org/hco/11/GRCh38#103479572-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6929169-A-C

103479653-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2962
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6929093-T-G