103594076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3 prime UTR variant
orthologous variants: 47248662-A-G

103594189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3 prime UTR variant
orthologous variants: 47248781-T-C

http://identifiers.org/hco/10/GRCh38#103594340-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47248930-A-C

103594340-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3 prime UTR variant
orthologous variants: 47248930-A-T

http://identifiers.org/hco/10/GRCh38#103594757-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47249288-A-C

http://identifiers.org/hco/10/GRCh38#103594850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47249358-C-A

103594850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3 prime UTR variant
orthologous variants: 47249358-C-T

103594905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3 prime UTR variant
orthologous variants: 47249401-T-C

http://identifiers.org/hco/10/GRCh38#103594990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47249478-C-A

103595102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3 prime UTR variant
orthologous variants: 47249568-G-A

103595194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3 prime UTR variant
orthologous variants: 47249640-G-T

103595439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3 prime UTR variant
orthologous variants: 47249803-T-C

103595502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3 prime UTR variant
orthologous variants: 47249862-G-A

103595617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3 prime UTR variant
orthologous variants: 47249957-G-A

103595617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3 prime UTR variant
orthologous variants: 47249957-G-T

103595896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3 prime UTR variant
orthologous variants: 47250218-C-T

103596039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3 prime UTR variant
orthologous variants: 47250323-A-G

http://identifiers.org/hco/10/GRCh38#103596142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47250430-C-A

http://identifiers.org/hco/10/GRCh38#103596162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47250456-C-A

103596187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3 prime UTR variant
orthologous variants: 47250478-G-T

103596191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3 prime UTR variant
orthologous variants: 47250482-G-A

http://identifiers.org/hco/10/GRCh38#103596192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47250483-C-A

103596192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3 prime UTR variant
orthologous variants: 47250483-C-T

103596227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3 prime UTR variant
orthologous variants: 47250518-C-T

http://identifiers.org/hco/10/GRCh38#103596304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47250560-C-A

103596307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3 prime UTR variant
orthologous variants: 47250563-T-C

103596569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3 prime UTR variant
orthologous variants: 47250818-A-G

103596662-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3 prime UTR variant
orthologous variants: 47250947-C-G

103597180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3 prime UTR variant
orthologous variants: 47251372-G-A

103597180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3 prime UTR variant
orthologous variants: 47251372-G-T

103597231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3 prime UTR variant
orthologous variants: 47251421-G-A

103597231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3 prime UTR variant
orthologous variants: 47251421-G-T

103597256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3 prime UTR variant
orthologous variants: 47251445-A-G

http://identifiers.org/hco/10/GRCh38#103597327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47251514-C-A

http://identifiers.org/hco/10/GRCh38#103597473-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47251627-C-A

103597473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3 prime UTR variant
orthologous variants: 47251627-C-T

103597825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3 prime UTR variant
orthologous variants: 47251883-T-C

103597878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3 prime UTR variant
orthologous variants: 47251931-G-T

http://identifiers.org/hco/10/GRCh38#103598473-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47252470-C-A

103598473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3 prime UTR variant
orthologous variants: 47252470-C-T

103598639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3 prime UTR variant
orthologous variants: 47252631-C-T

103598640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3 prime UTR variant
orthologous variants: 47252632-C-T

103598688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3 prime UTR variant
orthologous variants: 47252679-C-T

103598807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 47252787-G-A

http://identifiers.org/hco/10/GRCh38#103598828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#47252808-C-A

103598828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 47252808-C-T

103598832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 47252812-C-T

103598910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 47252882-G-T

103599077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 47253036-G-T

103599244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3 prime UTR variant
orthologous variants: 47253206-C-T

103599264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3 prime UTR variant
orthologous variants: 47253223-G-T

http://identifiers.org/hco/10/GRCh38#103599341-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47253276-C-A

103599341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3 prime UTR variant
orthologous variants: 47253276-C-T

103599378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3 prime UTR variant
orthologous variants: 47253313-G-A

103599378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3 prime UTR variant
orthologous variants: 47253313-G-T

103599546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47253454-T-C

http://identifiers.org/hco/10/GRCh38#103599656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47253567-C-A

103599941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47253840-G-T

103599947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47253845-G-A

103599947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47253845-G-T

http://identifiers.org/hco/10/GRCh38#103599950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47253848-C-A

103600070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47253907-G-A

http://identifiers.org/hco/10/GRCh38#103600206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47254043-C-A

103600206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47254043-C-T

103600220-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47254057-T-A

103600220-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47254057-T-G

103600243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47254082-T-C

103600244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47254083-G-A

103600244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47254083-G-T

http://identifiers.org/hco/10/GRCh38#103600351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47254190-C-A

103600355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47254194-G-A

103600360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47254199-G-T

103600362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47254201-C-T

103600417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47254249-C-T

103600454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47254278-C-T

103600480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47254297-T-C

103600640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47254368-T-C

http://identifiers.org/hco/10/GRCh38#103600875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47254567-C-A

103600875-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47254567-C-G

103600875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47254567-C-T

http://identifiers.org/hco/10/GRCh38#103600961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47254653-C-A

103601037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47254728-A-G

103601125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47254799-G-A

103601135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47254808-T-C

103601137-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47254810-T-G

http://identifiers.org/hco/10/GRCh38#103601194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47254866-C-A

103601368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47255031-G-A

103601368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47255031-G-T

103601398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47255061-C-T

103601416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47255077-G-A

103601416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47255077-G-T

http://identifiers.org/hco/10/GRCh38#103601454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47255110-C-A

103601454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47255110-C-T

103601537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47255181-T-C

http://identifiers.org/hco/10/GRCh38#103601583-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47255214-A-C

http://identifiers.org/hco/10/GRCh38#103601599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47255229-C-A

103601599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47255229-C-T

103601627-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47255257-T-A

103601627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47255257-T-C

103601748-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47255362-T-G

http://identifiers.org/hco/10/GRCh38#103601755-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47255369-A-C

103601755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47255369-A-G

http://identifiers.org/hco/10/GRCh38#103601757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47255371-C-A

103601757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47255371-C-T

http://identifiers.org/hco/10/GRCh38#103601960-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47255570-A-C

http://identifiers.org/hco/10/GRCh38#103602110-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47255720-A-C

103602119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47255729-G-A

103602119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47255729-G-T

103602143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47255753-G-A

103602143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47255753-G-T

103602158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47255768-A-G

103602293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47255903-C-T

103602317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47255927-C-T

103602347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47255957-G-A

103602368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47255978-G-A

103602404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47256014-G-A

103602404-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47256014-G-C

103602577-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47256181-T-G

103602620-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 47256224-C-G

103602626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47256230-G-A

103602626-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47256230-G-C

103602626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47256230-G-T

103602632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47256236-G-A

103602647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47256251-C-T

103602738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 47256342-G-T

103602800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47256392-C-T

103602801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 47256393-G-A

103602801-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 47256393-G-C

103602801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 47256393-G-T

103602949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 47256541-G-A

103602949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47256541-G-T

103603097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47256683-G-A

103603097-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47256683-G-C

103603115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47256701-G-A

103603162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 47256748-A-G

103603325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47256911-G-A

103603388-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 47256974-C-G

103603388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47256974-C-T

103603419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 47257005-C-T

103603451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47257037-G-A

http://identifiers.org/hco/10/GRCh38#103603459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47257045-C-A

103603459-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 47257045-C-G

103603459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 47257045-C-T

103603541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47257127-G-A

103603541-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 47257127-G-C

103603559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47257145-A-G

103603616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47257202-G-A

103603616-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47257202-G-C

http://identifiers.org/hco/10/GRCh38#103603646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47257232-C-A

103603646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47257232-C-T

103603664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47257250-G-T

103603845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47257430-A-G

103603846-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47257431-T-A

103603846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47257431-T-C

http://identifiers.org/hco/10/GRCh38#103603847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47257432-C-A

103603847-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47257432-C-G

103603847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47257432-C-T

http://identifiers.org/hco/10/GRCh38#103603892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47257439-C-A

103603892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47257439-C-T

103604191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47257680-A-G

103604306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47257782-T-C

103605603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47258117-G-A

103605734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47258243-G-A

103610161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47259004-A-G

103610161-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47259004-A-T

103610277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47259126-C-T

103610284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47259133-G-A

103610646-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47259480-G-C

http://identifiers.org/hco/10/GRCh38#103610929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47259843-C-A

103611157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47260053-C-T

103611163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47260059-C-T

103611451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47260335-A-G

103611546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47260423-G-A

103611546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47260423-G-T

103611644-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47260510-C-G

103611644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47260510-C-T

103611649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47260515-C-T

103611729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47260587-G-T

103611746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47260604-G-T

103611761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47260619-T-C

103611928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47260758-T-C

103612739-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47261512-G-C

103612739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47261512-G-T

103612827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47261598-G-T

http://identifiers.org/hco/10/GRCh38#103613046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47261813-C-A

103613046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47261813-C-T

103613085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47261852-C-T

103613208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47261974-A-G

103613274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47262044-G-A

103613274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47262044-G-T

103613281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47262051-G-A

103613281-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47262051-G-T

103613282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47262052-G-T

http://identifiers.org/hco/10/GRCh38#103613322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47262094-C-A

103613322-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47262094-C-G

103613322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47262094-C-T

103613329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47262101-G-A

103613329-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47262101-G-C

103613329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47262101-G-T

103613644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47262328-G-A

http://identifiers.org/hco/10/GRCh38#103613645-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47262329-A-C

103613645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47262329-A-G

103613760-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47262392-T-G

103614903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47264824-T-C

103614921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47264842-G-A

103614921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47264842-G-T

103615320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47265197-C-T

103615485-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47265371-T-G

103615553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47265444-A-G

103615880-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47265820-C-G

103616125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47266004-A-G

103616158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47266042-G-A

103616187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47266071-C-T

103616466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47266286-G-T

103616706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47266477-T-C

103616711-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47266482-G-C

103617127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47266713-G-A

103617127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47266713-G-T

103617144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47266733-C-T

103617323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47266885-G-T

103617345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47266908-T-C

103617373-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47266937-T-A

103617373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47266937-T-C

103617412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47266972-G-A

103617412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47266972-G-T

http://identifiers.org/hco/10/GRCh38#103617413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47266973-C-A

103617413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47266973-C-T

103617414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47266974-T-C

http://identifiers.org/hco/10/GRCh38#103617452-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47267009-A-C

103617452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47267009-A-G

103617452-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47267009-A-T

http://identifiers.org/hco/10/GRCh38#103617466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47267021-C-A

103617509-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47267062-T-A

103618439-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47267726-T-G

103618495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47267787-C-T

103618535-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47267804-T-A

103618588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47267831-G-A

103619390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47268562-C-T

103619634-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47268793-C-G

103620040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47269146-G-A

103620082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47269204-C-T

103620113-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47269236-T-G

103620186-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47269307-T-A

103620452-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47269564-C-G

103620706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47269794-G-A

103620706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47269794-G-T

103620777-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47269845-C-G

103620799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47269862-G-A

103620916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47269946-G-A

103621135-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47270133-A-T

103621262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47270276-C-T

103621355-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47270399-T-A

103621355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47270399-T-C

103621557-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47270581-G-C

103621747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47270801-G-A

103621754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47270808-G-A

103621988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47271019-G-A

103622239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47271237-A-G

103622312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47271317-C-T

103622322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47271323-G-A

103622322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47271323-G-T

103622498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 47271488-G-A

103622498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 47271488-G-T

103622654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47271641-G-A

103622654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47271641-G-T

http://identifiers.org/hco/10/GRCh38#103622656-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47271643-A-C

103622656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47271643-A-G

103622656-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47271643-A-T

103622685-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47271677-A-T

103622997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47271810-T-C

103623064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47271876-G-A

http://identifiers.org/hco/10/GRCh38#103623278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47272043-C-A

103623278-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47272043-C-G

103623278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47272043-C-T

103623465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47272209-C-T

103623536-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47272276-G-C

http://identifiers.org/hco/10/GRCh38#103626028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47274096-C-A

103626311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47274328-G-A

103626449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47274472-C-T

103626937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47274888-T-C

http://identifiers.org/hco/10/GRCh38#103627017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47274947-C-A

103627017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47274947-C-T

103627019-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47274949-A-T

http://identifiers.org/hco/10/GRCh38#103627025-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47274955-A-C

103627025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47274955-A-G

103627047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47274977-A-G

103627047-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47274977-A-T

103627159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47275114-A-G

103627186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47275141-G-A

103627186-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 47275141-G-C

103627186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 47275141-G-T

103627270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47275256-A-G

103627277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47275263-G-A

103627277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47275263-G-T

103627280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47275266-T-C

103627471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47275430-T-C

103627527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47275494-G-A

103627587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47275528-A-G

103627641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47275576-G-A

103627647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47275582-C-T

103627668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47275601-G-A

103627684-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47275618-C-G

103627684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47275618-C-T

103627685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47275619-G-A

103627737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47275671-G-A

103627737-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47275671-G-T

http://identifiers.org/hco/10/GRCh38#103627859-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47275800-A-C

http://identifiers.org/hco/10/GRCh38#103628024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47275960-C-A

103628024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47275960-C-T

103628090-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47275992-G-C

103628116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47276014-G-A

103628148-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47276047-G-C

103628276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47276156-G-T

http://identifiers.org/hco/10/GRCh38#103628284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47276164-C-A

103628284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47276164-C-T

103628619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47276448-G-A

103629107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47276594-A-G

103629290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47276752-G-A

103629465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47276928-C-T

103629551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47277004-G-T

103629779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47277213-C-T

103629788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47277219-G-A

103629820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47277251-G-A

103629832-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47277263-C-G

103629841-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47277273-C-G

103629851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47277284-C-T

103629862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47277295-G-A

103632646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47278197-C-T

103636461-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47279651-T-A

103636463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47279653-C-T

103636520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47279709-G-A

103636583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47279790-G-T

103636666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47279873-C-T

103636825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47280062-C-T

103637107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47280248-A-G

http://identifiers.org/hco/10/GRCh38#103637329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47280434-C-A

103637370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47280478-C-T

103637455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47280553-G-A

103637455-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47280553-G-C

103637643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47280722-G-A

103637693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47280773-G-A

103637716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47280800-G-A

103637746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47280809-C-T

103638302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47281349-C-T

103638482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47281517-T-C

103638530-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47281558-C-G

103638530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47281558-C-T

103638818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47281859-C-T

103639030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47282176-C-T

103639115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47282265-C-T

103639158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47282307-G-T

103641002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47282600-T-C

103641005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47282603-G-A

103641651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47283749-G-A

103641796-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47283869-T-A

103641796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47283869-T-C

http://identifiers.org/hco/10/GRCh38#103641838-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47283911-A-C

103641859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47283933-T-C

103641876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47283950-C-T

103642021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47284095-G-A

103642039-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47284118-C-G

103642261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47284931-A-G

103642314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47284980-G-A

103642356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47285021-G-T

103642420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47285065-C-T

103642493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47285142-T-C

103642508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47285171-T-C

103642627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47285284-A-G

103642653-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47285306-A-T

103642686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47285348-G-A

103642686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47285348-G-T

http://identifiers.org/hco/10/GRCh38#103642798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47285732-C-A

103642841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47285782-C-T

103642954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47285881-T-C

103642974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47285901-G-A

http://identifiers.org/hco/10/GRCh38#103643056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47285983-C-A

103643056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47285983-C-T

103643139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47286066-C-T

103643209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47286136-G-A

103643538-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47286409-G-C

103643541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47286412-C-T

103643571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47286435-G-A

103643650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47286498-A-G

103644966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47286826-A-G

103645234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47287154-G-T

103645607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47287495-G-A

103645717-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47287602-G-C

103645764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47287646-C-T

http://identifiers.org/hco/10/GRCh38#103645785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47287663-C-A

http://identifiers.org/hco/10/GRCh38#103645948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47287828-C-A

103646114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47287972-C-T

http://identifiers.org/hco/10/GRCh38#103646371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47288194-C-A

103646371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47288194-C-T

103646501-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47288292-A-T

103646661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47288375-G-A

103646733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47288433-C-T

103646801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47288486-C-T

http://identifiers.org/hco/10/GRCh38#103646954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47288588-C-A

103646983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47288614-G-A

103646997-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47288628-T-G

http://identifiers.org/hco/10/GRCh38#103647101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47288751-C-A

103647101-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47288751-C-G

103647101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47288751-C-T

103647182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47288835-C-T

103647250-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47288889-T-G

103647254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47288893-A-G

http://identifiers.org/hco/10/GRCh38#103647346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47288981-C-A

103647454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47289066-A-G

103647728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47289308-A-G

103647878-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47289403-C-G

103647879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47289404-T-C

103648146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47289609-G-A

103648224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47289689-C-T

103648316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47289789-C-T

103648871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47290296-A-G

103648934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47290347-T-C

103649090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47290500-C-T

http://identifiers.org/hco/10/GRCh38#103649177-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47290601-A-C

103649224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47290646-T-C

103649421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47290829-T-C

103649458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47290872-G-A

http://identifiers.org/hco/10/GRCh38#103649584-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47290998-A-C

103650014-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47291384-T-A

103650096-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47291438-G-C

http://identifiers.org/hco/10/GRCh38#103650223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47291535-C-A

103650502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47291702-T-C

103650575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47291741-C-T

103650606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47291772-G-A

103650727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47291865-C-T

103650731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47291869-G-A

103650733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47291871-C-T

103650766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47291905-G-A

103650808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47291934-G-A

103650888-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47291997-T-A

103651060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47292126-A-G

103651156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47292217-A-G

103651238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47292288-C-T

103651432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47292435-G-A

103651538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47292540-C-T

103651549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47292549-T-C

103651615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47292615-T-C

103651644-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47292644-C-G

103651644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47292644-C-T

103651659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47292659-C-T

103651709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47292709-G-A

103651857-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47292859-T-G

103651923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47292916-C-T

103652247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47293231-G-A

103652247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47293231-G-T

103652660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47293642-G-A

103652689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47293672-C-T

103652709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47293692-G-A

103652770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47293785-G-A

103653620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47293910-G-T

103653635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47293925-T-C

103653655-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47293944-T-A

103653655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47293944-T-C

103654095-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47294317-C-G

103654124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47294346-G-A

103654124-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47294346-G-C

103654260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47294395-G-A

http://identifiers.org/hco/10/GRCh38#103654394-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47294511-A-C

103654717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47294859-C-T

103654926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47295059-C-T

103654969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47295102-C-T

103655056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47295172-G-A

103655150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47295266-G-A

http://identifiers.org/hco/10/GRCh38#103655208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47295324-C-A

103655208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47295324-C-T

103655225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47295342-C-T

http://identifiers.org/hco/10/GRCh38#103655291-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47295401-A-C

103655303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47295413-C-T

103655547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47295636-T-C

103655925-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47295938-C-G

103657057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47298207-G-T

103657123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47298261-G-A

103657202-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47298339-T-G

http://identifiers.org/hco/10/GRCh38#103657209-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47298345-A-C

103657214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47298350-G-T

103657556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47298742-C-T

http://identifiers.org/hco/10/GRCh38#103657948-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47299409-A-C

103658442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47299940-C-T

http://identifiers.org/hco/10/GRCh38#103658563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47300073-C-A

103658828-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47300304-T-G

103659254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47300844-G-T

103659301-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47300890-G-C

103659345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47300934-T-C

103659892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47301371-C-T

103660064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47301526-C-T

103660123-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47301583-T-G

103660226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47301686-C-T

103660246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47301701-G-A

103660652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47302149-T-C

103660696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47302190-G-A

103660961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47302464-G-A

103660961-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47302464-G-C

103661158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 47302649-G-A

103661158-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 47302649-G-C

http://identifiers.org/hco/10/GRCh38#103661230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47302718-C-A

103661264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47302752-A-G

103661264-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47302752-A-T

http://identifiers.org/hco/10/GRCh38#103661360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47302848-C-A

103661360-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47302848-C-G

103661441-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47302932-A-T

103661473-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47302964-G-C

103661541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47303022-G-A

103661541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47303022-G-T

103661665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47303171-G-A

103661665-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47303171-G-C

103661758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47303245-G-A

103661827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47303314-G-A

103661888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47303374-G-A

103662044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47303501-G-A

103662159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47303614-G-T

103663335-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47304250-T-G

103663431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47304346-C-T

103663445-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47304360-C-G

103663473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47304381-T-C

103663560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47304496-T-C

103663640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47304572-T-C

103663689-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47304620-T-A

103663689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47304620-T-C

103663740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47304657-C-T

103663748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47304665-T-C

103664100-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47304994-C-G

103664462-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47305277-T-G

103664547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47305351-C-T

103664577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47305380-C-T

103664753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47305404-G-A

103665015-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47305501-C-G

103665015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47305501-C-T

103665150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47305615-G-A

103665152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47305617-G-A

103665365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47305832-C-T

http://identifiers.org/hco/10/GRCh38#103665573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47306016-C-A

103665804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47306213-G-A

http://identifiers.org/hco/10/GRCh38#103665929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47306320-C-A

103666016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47306390-G-A

103666114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47306500-C-T

103666115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47306501-G-A

103666214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47306597-A-G

103666325-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47306684-C-G

103667522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47307756-G-A

103667930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47308090-C-T

103668171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47308318-A-G

103668226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47308367-C-T

103668242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47308382-G-A

http://identifiers.org/hco/10/GRCh38#103668479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47308607-C-A

103668479-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47308607-C-G

103668491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47308617-G-T

http://identifiers.org/hco/10/GRCh38#103668536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47308648-C-A

103668536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47308648-C-T

103668537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47308649-A-G

103668537-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47308649-A-T

103668601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 47308708-G-A

103668601-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 47308708-G-C

103668601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 47308708-G-T

103669025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47309098-G-A

103669316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47309568-C-T

103669366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47309619-G-A

103669462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47309733-G-A

103669514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47309935-G-A

http://identifiers.org/hco/10/GRCh38#103669794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47310187-C-A

103669794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47310187-C-T

103670242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47310577-T-C

103670724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47311131-G-A

103671025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47311286-T-C

103671111-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47311333-C-G

103671111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47311333-C-T

103671276-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47311547-A-T

103671438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47311886-C-T

103671943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47312245-C-T

103672838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47313723-C-T

103673028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47313904-G-A

103673029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47313905-A-G

103673762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47314133-A-G

103673764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47314135-G-A

103673764-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47314135-G-C

103673974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47314300-A-G

103673975-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47314301-T-A

103674059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47314362-G-A

103674258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47314549-C-T

103675011-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47315208-C-G

103675092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47315273-G-A

103675320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47315481-T-C

103675556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47315690-G-T

103676292-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47316227-G-C

103676325-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47316260-G-C

103676437-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47316348-C-G

103676518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47316407-G-A

103676627-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47316478-T-A

103676787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47316634-C-T

103676942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47317018-G-A

103676942-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47317018-G-C

103677106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47317197-A-G

103677302-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47317405-T-A

http://identifiers.org/hco/10/GRCh38#103677992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47318959-C-A

103677992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47318959-C-T

103677993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47318960-A-G

103678055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47319009-T-C

103678071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47319021-G-T

103678096-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47319069-T-A

103678096-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47319069-T-G

103678105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47319078-G-T

103678124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 47319097-C-T

http://identifiers.org/hco/10/GRCh38#103678147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47319120-C-A

103678147-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47319120-C-G

103678147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47319120-C-T

103678317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47319295-C-T

103678326-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47319304-A-T

http://identifiers.org/hco/10/GRCh38#103678724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47319665-C-A

103679148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47321256-C-T

103679149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47321257-C-T

103679450-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47321546-A-T

103679452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47321548-G-A

103679483-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47321571-C-G

103679773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47321823-C-T

103679815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47321861-C-T

103680768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47322215-T-C

103681048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47322493-G-A

103681090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47322535-A-G

103681288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47322723-A-G

103681370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47322776-C-T

103681389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47322797-C-T

http://identifiers.org/hco/10/GRCh38#103681423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47322820-C-A

http://identifiers.org/hco/10/GRCh38#103681458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47322855-C-A

103681458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47322855-C-T

103682128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47323145-G-A

103682267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47323259-C-T

103682340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47323336-G-A

http://identifiers.org/hco/10/GRCh38#103682813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47323491-C-A

103682813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47323491-C-T

http://identifiers.org/hco/10/GRCh38#103683854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47323884-C-A

103684172-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47324062-G-C

http://identifiers.org/hco/10/GRCh38#103684179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47324069-C-A

103684288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47324143-G-A

http://identifiers.org/hco/10/GRCh38#103684311-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47324161-A-C

103685956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47326084-C-T

103687844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47326958-T-C

103687852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47326966-A-G

103687991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47327050-A-G

103688015-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47327074-A-T

103688182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47327234-C-T

103688191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47327246-C-T

103688200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47327255-T-C

103688259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47327305-C-T

103688644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47327614-G-A

103688710-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47327680-C-G

103688781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47327749-G-A

103688783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47327751-G-A

103690336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47329433-G-A

103690417-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47329508-G-C

103690424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47329515-T-C

103690739-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47329850-T-A

103690894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47329999-T-C

103691716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47330643-G-A

103691961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47330872-C-T

103691962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47330873-A-G

103692081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47331004-C-T

103692701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47331593-G-A

103692730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47331622-C-T

103692904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47331770-G-A

103692904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47331770-G-T

http://identifiers.org/hco/10/GRCh38#103692945-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47331806-A-C

103692973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47331836-G-A

103692973-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47331836-G-C

103692973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47331836-G-T

http://identifiers.org/hco/10/GRCh38#103692974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47331837-C-A

103692974-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47331837-C-G

103692974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47331837-C-T

http://identifiers.org/hco/10/GRCh38#103692980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47331843-C-A

103692980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47331843-C-T

http://identifiers.org/hco/10/GRCh38#103693188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47332037-C-A

103693188-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47332037-C-G

103693188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47332037-C-T

103693227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47332079-G-A

103693227-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47332079-G-C

103693227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47332079-G-T

http://identifiers.org/hco/10/GRCh38#103693234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47332086-C-A

103693234-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47332086-C-G

103693234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47332086-C-T

103693241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47332093-C-T

http://identifiers.org/hco/10/GRCh38#103693307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47332215-C-A

http://identifiers.org/hco/10/GRCh38#103693332-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47332233-A-C

103693332-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 47332233-A-T

103693471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47332320-C-T

http://identifiers.org/hco/10/GRCh38#103693483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47332326-C-A

103693483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 47332326-C-T

103693493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47332336-C-T

http://identifiers.org/hco/10/GRCh38#103693531-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47332356-A-C

http://identifiers.org/hco/10/GRCh38#103693569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47332388-C-A

103693602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 47332396-G-T

103693606-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47332400-G-C

http://identifiers.org/hco/10/GRCh38#103693637-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47332406-A-C

103693657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47332424-A-G

103693657-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47332424-A-T

103693731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47332520-A-G

103693767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47332546-G-A

103693767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47332546-G-T

103693839-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47332617-A-T

103693887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47332669-C-T

103693937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47332721-G-A

103694365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47333070-T-C

103694540-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47333187-G-C

103694600-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47333219-C-G

103694744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47333336-C-T

103694770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47333361-C-T

103694842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47333423-C-T

103695224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47334005-G-T

103695229-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47334010-T-A

103695229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47334010-T-C

http://identifiers.org/hco/10/GRCh38#103695317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47334110-C-A

103695317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47334110-C-T

103695484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47334286-G-A

http://identifiers.org/hco/10/GRCh38#103695498-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47334300-A-C

http://identifiers.org/hco/10/GRCh38#103695501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47334305-C-A

103695501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47334305-C-T

http://identifiers.org/hco/10/GRCh38#103695507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47334311-C-A

103695533-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47334329-T-A

103695533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47334329-T-C

103695533-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47334329-T-G

103695603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47334398-C-T

103695898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47334667-G-A

103695898-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47334667-G-C

103696247-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47334990-C-G

103696463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47335201-G-A

103696466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47335204-G-A

103696558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47335238-G-A

103696709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47335382-G-A

103696858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47335502-A-G

103697098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47335677-G-A

103697098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47335677-G-T

103697206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47335752-C-T

103697390-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47336407-C-G

103698303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47337177-C-T

103698315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47337189-C-T

103698348-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47337222-C-G

103698376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47337245-C-T

103698453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47337322-C-T

103698491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47337363-C-T

103698916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47337742-C-T

103698926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47337752-G-A

103699075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47337897-G-A

103699087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47337909-G-A

103699087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47337909-G-T

http://identifiers.org/hco/10/GRCh38#103699505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47339122-C-A

103699618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47339223-T-C

103699658-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47339263-T-A

103699718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47339323-G-A

http://identifiers.org/hco/10/GRCh38#103700213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47339839-C-A

103700367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47339956-A-G

103700555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47340109-C-T

103700562-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47340116-G-C

103700562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47340116-G-T

103700702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47340195-C-T

103700724-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47340217-C-G

103700725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47340218-C-T

103700772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47340262-T-C

103700775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47340265-T-C

103700857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47340327-G-A

103700920-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47340374-C-G

103700920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47340374-C-T

http://identifiers.org/hco/10/GRCh38#103700980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47340436-C-A

103700991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47340447-C-T

103701024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47340482-C-T

103702255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47340527-G-A

103702398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47340660-T-C

103702438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47340700-G-A

103702553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47340813-G-T

103702566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47340826-G-A

103702566-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47340826-G-C

103702816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47340905-T-C

103703272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47341205-T-C

103703341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47341285-G-A

103703401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47341345-C-T

103703569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47341532-T-C

103704105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47342657-C-T

103704197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47342734-C-T

103704230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47342760-G-A

103704261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47342785-C-T

103704543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47343032-C-T

103704552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47343041-T-C

103704752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47343233-C-T

103704785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47343272-G-A

103708392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47344151-T-C

103708419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47344169-G-A

103708511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47344276-G-A

103714205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47346271-C-T

103714220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47346286-A-G

103714309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47346401-A-G

103714331-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47346423-C-G

103714617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47346660-C-T

103714873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47346915-C-T

103714939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47346960-C-T

103714966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47346987-G-T

103714967-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47346988-T-G

103714972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47346993-G-A

103715100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47347073-T-C

103715324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47347167-G-A

103715550-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47347377-C-G

103715550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47347377-C-T

103715862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47347641-G-A

103716000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47347767-G-A

103716061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47347842-T-C

103716061-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47347842-T-G

103716078-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47347859-C-G

103716078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47347859-C-T

103716112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47347878-C-T

103716151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47347920-G-A

103716163-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47347932-C-G

103716545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47348323-A-G

103716550-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47348328-A-T

103720276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47351197-C-T

103720355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47351276-G-T

103720426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47351316-G-A

103720429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47351320-G-A

103720429-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47351320-G-C

103720429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47351320-G-T

103720500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47351376-A-G

103720519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47351381-C-T

http://identifiers.org/hco/10/GRCh38#103720588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47351448-C-A

103720712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47351570-T-C

103720866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47351718-G-A

103720878-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47351726-C-G

103720878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47351726-C-T

103720879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47351727-G-A

103720893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47351743-G-A

http://identifiers.org/hco/10/GRCh38#103721109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#47351864-C-A

103721109-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47351864-C-G

103721112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47351867-C-T

103721118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47351873-G-A

103721303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47352041-G-A

http://identifiers.org/hco/10/GRCh38#103721357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47352091-C-A

103721357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47352091-C-T

103721383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47352117-G-A

103721621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47352320-C-T

103721656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47352344-G-A

103724218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47353025-G-A

103724218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47353025-G-T

http://identifiers.org/hco/10/GRCh38#103724229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47353036-C-A

103724229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47353036-C-T

103724257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47353049-A-G

103724257-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47353049-A-T

103724286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 47353078-C-T

103724371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47353162-G-A

103724371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47353162-G-T

103724385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47353176-G-A

103724385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47353176-G-T

103724391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47353182-G-A

103724391-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47353182-G-C

103724391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47353182-G-T

103724395-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47353186-T-G

http://identifiers.org/hco/10/GRCh38#103724459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47353242-C-A

103724887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47353864-A-G

103725030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47354033-A-G

103725086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47354089-G-A

http://identifiers.org/hco/10/GRCh38#103727267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47354708-C-A

103727382-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47354821-C-G

103727422-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47354887-C-G

103727422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47354887-C-T

103727516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47354961-C-T

103727683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47355058-G-A

103727687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47355062-G-A

103727714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47355089-G-A

103727715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47355090-C-T

103727716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47355091-G-A

103727725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47355096-G-A

103727761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47355127-C-T

103727918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47355234-T-C

103727975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47355285-C-T

103727988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47355298-C-T

103727990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47355300-T-C

103728085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47355365-G-A

103728187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47355419-C-T

103728202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47355434-T-C

103728285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47355514-A-G

103728294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47355523-G-A

103728619-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47355821-C-G

103728720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47355913-T-C

103733051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47358143-T-C

103733104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47358188-T-C

103733148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47358234-T-C

103733176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47358262-G-A

103733190-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47358281-T-A

http://identifiers.org/hco/10/GRCh38#103733590-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47358602-A-C

103733678-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47358675-A-T

103733695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47358698-C-T

http://identifiers.org/hco/10/GRCh38#103734933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47360933-C-A

103734933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47360933-C-T

103735105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47361090-G-A

103735509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47361604-T-C

103735577-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47361676-T-G

103735585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47361703-T-C

103735656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47361771-A-G

103735675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47361792-C-T

103736715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47362847-C-T

103736721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47362853-G-A

103736721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47362853-G-T

103736780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 47362895-C-T

103736995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47363045-C-T

103737216-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47363253-C-G

103737216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47363253-C-T

103737391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47363291-C-T

103737414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47363314-A-G

103737621-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47363526-G-C

103737627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47363532-T-C

103737898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47363742-C-T

103737976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47363770-C-T

103738073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47363870-C-T

103738420-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47364161-G-C

103738462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47364201-T-C

103738525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47364246-G-A

103738548-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47364270-T-G

103739178-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47364525-T-A

103739461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47364750-G-A

103739726-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, undefined
orthologous variants: 47364998-C-G

103739726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, undefined
orthologous variants: 47364998-C-T

103739964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47365217-C-T

103746990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47367379-T-C

103747020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47367397-G-A

103747035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47367412-G-A

103747035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47367412-G-T

103747079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47367456-A-G

http://identifiers.org/hco/10/GRCh38#103747147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47367531-C-A

103747147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47367531-C-T

103747149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47367533-T-C

103747217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47367594-T-C

103747233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47367600-A-G

103747298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47367667-C-T

103747367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47367729-T-C

103747399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47367758-G-A

103747461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47367820-G-A

http://identifiers.org/hco/10/GRCh38#103748250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47368365-C-A

103748250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47368365-C-T

103748778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47368673-G-A

103748831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47368727-A-G

103749000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47368938-C-T

http://identifiers.org/hco/10/GRCh38#103749049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47368964-C-A

103749077-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47368992-G-C

103749081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47369000-G-A

103749110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47369022-C-T

103749361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47369294-G-A

http://identifiers.org/hco/10/GRCh38#103749542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47369395-C-A

103749542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47369395-C-T

103749574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47369426-C-T

103751816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47369762-C-T

103751848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47369793-A-G

103751954-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47369899-T-A

103752030-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47369972-G-C

103752068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47370006-G-A

http://identifiers.org/hco/10/GRCh38#103752505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47370402-C-A

103752788-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47370665-G-C

103753069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47371051-G-A

103753111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47371091-T-C

http://identifiers.org/hco/10/GRCh38#103753903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47371541-C-A

103754160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47371751-G-A

http://identifiers.org/hco/10/GRCh38#103754523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47372186-C-A

103754523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47372186-C-T

103754537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47372202-G-T

103754611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47372274-G-A

103754611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47372274-G-T

http://identifiers.org/hco/10/GRCh38#103754652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47372292-C-A

103754684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47372323-G-T

http://identifiers.org/hco/10/GRCh38#103754813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47372455-C-A

103754843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47372478-G-T

103754876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47372513-G-T

103754884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47372521-T-C

103754916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47372553-G-T

103754920-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47372561-C-G

103754923-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47372564-T-A

103754923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47372564-T-C

103754923-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47372564-T-G

103754946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47372587-G-T

http://identifiers.org/hco/10/GRCh38#103755071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47372689-C-A

103755162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47372762-G-A

103755162-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47372762-G-C

103755162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47372762-G-T

103755300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47372885-G-T

103755305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47372890-T-C

103755316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47372900-C-T

103755380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47372931-T-C

103755394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47372945-G-T

103755417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47372956-T-C

103755568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47372962-T-C

103755728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47373165-G-A

103755851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47373222-G-A

103755860-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47373231-T-A

103755941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47373264-T-C

103756139-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47373453-G-C

http://identifiers.org/hco/10/GRCh38#103756218-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47373498-A-C

http://identifiers.org/hco/10/GRCh38#103756450-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47373694-A-C

http://identifiers.org/hco/10/GRCh38#103756573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47373806-C-A

103756573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47373806-C-T

103756675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47373902-C-T

103756676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47373903-A-G

103756686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47373913-C-T

103756742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47373977-C-T

103756840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47374083-C-T

http://identifiers.org/hco/10/GRCh38#103757134-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47374480-A-C

103757288-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47374618-C-G

103757594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47374910-G-A

103757614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47374929-A-G

103757624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47374944-A-G

103757645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47374965-C-T

103757691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47374993-G-A

103757701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47375003-C-T

103757706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47375008-C-T

103758130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47375058-C-T

103758170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47375109-C-T

103758237-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47375167-T-A

103758315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47375231-G-A

103758537-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47375451-C-G

http://identifiers.org/hco/10/GRCh38#103758652-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47375571-A-C

103758668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47375587-C-T

103758669-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47375588-C-G

103758669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47375588-C-T

103758671-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47375590-T-A

103758671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47375590-T-C

103758741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47375636-A-G

http://identifiers.org/hco/10/GRCh38#103758965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47375823-C-A

http://identifiers.org/hco/10/GRCh38#103759021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47375877-C-A

103759195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47376041-C-T

103759304-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47376153-C-G

103759337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47376186-G-A

103759347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47376196-G-A

103759419-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47376269-G-C

103759441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47376292-G-A

103759506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47376355-C-T

103759611-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47376460-C-G

http://identifiers.org/hco/10/GRCh38#103759769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47376620-C-A

103759769-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47376620-C-G

103759925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47376731-T-C

103761490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47379348-G-T

103762613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47380784-T-C

103762811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47380941-T-C

103763044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47381161-G-T

http://identifiers.org/hco/10/GRCh38#103763151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47381268-C-A

103763210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47381326-C-T

103763296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47381405-C-T

103763315-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47381419-C-G

103764908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47383011-G-A

103765074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47383177-G-A

103765114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47383216-T-C

http://identifiers.org/hco/10/GRCh38#103765207-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47383290-A-C

103765207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47383290-A-G

103765301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47383356-G-A

103765377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47383427-A-G

103765591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47383823-T-C

http://identifiers.org/hco/10/GRCh38#103765828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47384079-C-A

103766017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47384224-T-C

103766059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47384253-G-A

103766162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47384341-C-T

103766423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47384559-C-T

http://identifiers.org/hco/10/GRCh38#103766449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47384585-C-A

103766536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47384676-G-T

103766608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47384748-C-T

103766616-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47384756-C-G

103766616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47384756-C-T

103766675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47384846-T-C

103766681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47384868-G-A

103766683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47384870-C-T

103766689-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47384876-G-C

103766910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47386106-G-A

103766962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47386157-G-A

http://identifiers.org/hco/10/GRCh38#103766989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47386163-C-A

103767074-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47386235-T-G

103767191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47386352-G-A

103767191-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47386352-G-C

103767191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47386352-G-T

103767294-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47386424-T-A

103767294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47386424-T-C

http://identifiers.org/hco/10/GRCh38#103767306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47386436-C-A

103767371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47386497-G-A

103767371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47386497-G-T

103767416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47386527-G-A

103767430-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47386541-C-G

103767430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47386541-C-T

103767448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47386559-T-C

103767451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47386562-G-A

103767459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47386571-G-T

103767531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47386640-T-C

103767666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47386777-T-C

103767689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47386800-T-C

103767916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47387009-G-A

103767916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47387009-G-T

103768088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47387118-A-G

103768119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47387141-T-C

103768509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47387493-G-A

103768510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47387494-G-A

103769173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47387521-T-C

103769196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47387543-A-G

103770161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47388270-C-T

103770169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47388278-A-G

103770431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47388459-C-T

103770723-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47388703-A-T

103771013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47388932-T-C

103771031-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47388950-G-C

103771315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47389348-T-C

103771377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47389414-A-G

103771413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47389443-C-T

103771419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47389449-C-T

103771957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47390972-A-G

103772130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47391152-G-A

103772130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47391152-G-T

103772131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47391153-G-A

103772311-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47391296-T-A

103772449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47391427-T-C

103772748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47391711-C-T

103777435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47395963-C-T

103777817-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47396289-G-C

103778873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47396968-G-T

103779514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47397290-G-A

103779748-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47397516-G-C

103779789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47397534-G-A

103779789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47397534-G-T

103779804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47397555-C-T

103779897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47397633-T-C

103779968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47397724-C-T

103779969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47397725-G-A

103780387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47398219-T-C

103780442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47398273-C-T

103780684-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47398531-C-G

http://identifiers.org/hco/10/GRCh38#103780799-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47398625-A-C

103781062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47398834-C-T

103781086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47398855-T-C

103781255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47399003-A-G

103781827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47399440-G-A

103782130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47399687-G-A

103782208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47399761-G-A

103782339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47399894-G-A

http://identifiers.org/hco/10/GRCh38#103782552-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47400094-A-C

103782617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47400152-A-G

103782771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47400259-A-G

103782771-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47400259-A-T

http://identifiers.org/hco/10/GRCh38#103782815-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47400298-A-C

103782815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47400298-A-G

103782873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47400313-G-A

103782873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47400313-G-T

103782920-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47400367-T-G

103783100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47400532-C-T

103783202-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47400613-T-G

103783211-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47400623-C-G

103783211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47400623-C-T

103783264-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47400677-G-C

103783335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47400709-T-C

103783696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47400964-T-C

103783767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47401034-A-G

103783767-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47401034-A-T

103783770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47401037-A-G

103783872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47401142-C-T

103783924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47401181-A-G

103784014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47401264-C-T

103784016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47401266-G-A

103784016-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47401266-G-C

103784240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47401448-C-T

103784297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47401496-C-T

103784484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47401674-T-C

103784703-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47401847-T-G

103785166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47402249-C-T

103787401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47402644-C-T

103787570-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47402819-G-C

103787740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47402969-G-A

103787816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47403033-C-T

103787837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47403078-G-A

103788122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47403333-C-T

103788126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47403337-G-A

http://identifiers.org/hco/10/GRCh38#103788291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47403508-C-A

103788974-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47403819-G-C

103789111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47403923-C-T

http://identifiers.org/hco/10/GRCh38#103789123-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47403935-A-C

103789179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47403975-G-A

103789179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47403975-G-T

103789227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47404023-A-G

http://identifiers.org/hco/10/GRCh38#103789258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47404048-C-A

103789258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47404048-C-T

103789298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47404087-G-T

103789368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47404145-C-T

103789372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47404149-G-A

103789472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47404210-C-T

103789480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47404218-A-G

103789536-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47404393-C-G

103789675-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47404571-A-T

103789762-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47404652-T-A

103789789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47404680-C-T

103789932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47404824-C-T

103790120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47404980-C-T

103790390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47405329-G-A

103790400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47405336-C-T

103790401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47405337-G-A

103790401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47405337-G-T

103790725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47405664-G-T

103790805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47405743-G-A

103790999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47405947-A-G

103791239-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47406184-T-A

103791255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47406211-A-G

103791469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47406336-G-A

103791501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47406350-T-C

103791574-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47406409-T-A

103791574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47406409-T-C

103791723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47406543-C-T

103791738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47406557-G-T

103791924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47406753-C-T

103791985-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47406823-G-C

http://identifiers.org/hco/10/GRCh38#103792015-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47406841-A-C

103792324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47407462-C-T

103792346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47407484-C-T

103792760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47407854-C-T

103792988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47408089-T-C

103792988-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47408089-T-G

103793223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47408274-A-G

http://identifiers.org/hco/10/GRCh38#103794018-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47409475-A-C

http://identifiers.org/hco/10/GRCh38#103794306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47409798-C-A

103794306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47409798-C-T

103794366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, undefined
orthologous variants: 47409859-C-T

103794501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, undefined
orthologous variants: 47409994-C-T

http://identifiers.org/hco/10/GRCh38#103799434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47410956-C-A

103799554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47411069-G-A

103799559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47411072-G-A

103800083-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47411665-C-G

103800246-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47411848-G-C

103800768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47412338-C-T

103800937-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47412498-C-G

103800963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47412522-G-A

103801076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47412631-C-T

http://identifiers.org/hco/10/GRCh38#103801147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47412801-C-A

103801147-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47412801-C-G

103801147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47412801-C-T

103801155-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47412809-T-A

103801155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47412809-T-C

103801256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47412904-C-T

103801261-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47412909-T-A

103801261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47412909-T-C

103801365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 47413012-G-T

103801454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47413091-G-A

103801454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47413091-G-T

103801516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47413135-T-C

http://identifiers.org/hco/10/GRCh38#103801524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47413143-C-A

http://identifiers.org/hco/10/GRCh38#103801572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47413205-C-A

103801639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47413269-T-C

103802545-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47413749-G-C

103802552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47413760-C-T

103802593-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47413804-G-C

103802606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47413819-C-T

103802818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47413949-A-G

103803178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47414593-G-A

103803207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47414621-T-C

http://identifiers.org/hco/10/GRCh38#103803244-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47414658-A-C

103804723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47416042-G-A

103804724-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47416043-C-G

103804733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47416050-A-G

103804802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47416120-C-T

103805083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47416365-G-A

103805083-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47416365-G-C

103805097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47416379-G-A

103805097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47416379-G-T

103805240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47416609-T-C

103806153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47416748-A-G

103806177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47416772-A-G

103806623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47417159-G-T

103806718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47417242-A-G

103806743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47417266-T-C

http://identifiers.org/hco/10/GRCh38#103806952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47417442-C-A

103806956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47417446-C-T

103807000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47417475-G-A

103807103-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47417596-C-G

103807125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47417616-G-T

103807152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47417635-G-A

http://identifiers.org/hco/10/GRCh38#103807154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47417637-C-A

103807154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47417637-C-T

103807258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47417706-C-T

103807461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47417903-A-G

103807494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47417949-T-C

103807526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47417982-A-G

103807537-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47417993-T-G

http://identifiers.org/hco/10/GRCh38#103808105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47418503-C-A

103811135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47419907-T-C

http://identifiers.org/hco/10/GRCh38#103811264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47420046-C-A

103812430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47420799-G-A

103812585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47420950-T-C

103812630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47420992-C-T

103812673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47421030-G-A

103812901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47421241-C-T

http://identifiers.org/hco/10/GRCh38#103813689-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47421952-A-C

103813690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47421953-G-A

103813802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47422061-T-C

103813984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47422251-G-A

103813984-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47422251-G-C

103814227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47422481-G-A

103814227-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47422481-G-C

103814417-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47422641-T-A

103814418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47422642-G-A

103814469-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47422690-C-G

103814522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47422743-C-T

103814553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47422768-T-C

103814835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47423030-T-C

103814853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47423045-G-A

103815160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47423361-T-C

103815161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47423362-G-A

103815200-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47423413-C-G

http://identifiers.org/hco/10/GRCh38#103815226-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47423439-A-C

103815226-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47423439-A-T

103818275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47424563-G-A

103818276-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47424564-G-C

http://identifiers.org/hco/10/GRCh38#103818513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47424786-C-A

103818677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47424945-G-A

103818677-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47424945-G-C

103819021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47425168-T-C

103819273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47425589-G-A

103819542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47425980-G-A

http://identifiers.org/hco/10/GRCh38#103819543-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47425981-A-C

103819591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47426012-G-A

103819646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47426066-T-C

103819714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47426132-T-C

103819951-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47426360-C-G

103820231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47426814-G-T

http://identifiers.org/hco/10/GRCh38#103820267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47426856-C-A

103820748-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47427283-C-G

103821054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47427566-T-C

103824105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47428587-C-T

103824176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47428669-G-A

103824365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47428828-G-A

103824492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47428937-T-C

103825345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47429691-T-C

103825380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47429722-A-G

103825472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47429820-T-C

103825557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47429921-C-T

103825605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47429970-C-T

103826753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47430292-G-A

103826968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47430477-G-A

103827024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47430524-G-T

103827201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47430699-A-G

103827447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47430911-G-A

103827470-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47430934-A-T

103827521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47430984-G-A

103827552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47431015-T-C

103827620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47431082-C-T

103827820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47431556-A-G

103827939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47431672-C-T

103827965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47431692-G-A

103828033-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47431754-T-A

103828160-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47431879-T-A

103828335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47432043-G-A

103828380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47432087-G-T

103828381-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47432088-T-A

103828520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47432209-G-A

http://identifiers.org/hco/10/GRCh38#103829633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47433104-C-A

103829633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47433104-C-T

103829691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47433167-G-A

103829691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47433167-G-T

103829839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47433612-G-A

103829966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47433731-G-A

103829982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47433747-G-A

103829998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47433762-C-T

http://identifiers.org/hco/10/GRCh38#103830000-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47433764-A-C

103830403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47434142-G-A

103830524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47434299-A-G

http://identifiers.org/hco/10/GRCh38#103830641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47434411-C-A

103830643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47434413-T-C

103833768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, undefined
orthologous variants: 47435434-G-T

103834082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, undefined
orthologous variants: 47435759-A-G

103834199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47435864-C-T

103836933-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47436464-C-G

103836933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47436464-C-T

103837000-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47436517-T-A

103837053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47436584-C-T

http://identifiers.org/hco/10/GRCh38#103837186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47436718-C-A

103837263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47436777-G-A

103837273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47436787-A-G

103837457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47436952-A-G

103837458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47436953-G-A

103838054-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47437177-C-G

103838127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47437256-C-T

103838260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47437382-C-T

103838324-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47437422-C-G

103838371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47437469-G-A

103838376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47437474-G-A

103838377-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47437475-G-C

103838402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47437501-A-G

103838513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47437600-A-G

103838964-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47438087-C-G

103839846-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47438901-C-G

103839915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47438954-G-A

103840712-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47439593-C-G

103840851-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47439698-G-C

103840902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47439750-G-A

103840926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47439775-A-G

http://identifiers.org/hco/10/GRCh38#103840983-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47439837-A-C

103841035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47439891-T-C

103841417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47440213-C-T

http://identifiers.org/hco/10/GRCh38#103841619-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#47440376-A-C

http://identifiers.org/hco/10/GRCh38#103841645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#47440415-C-A

103843240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47441240-G-A

103843291-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47441293-T-G

103843425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47441426-C-T

103843463-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47441476-T-A

103843463-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47441476-T-G

103843479-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47441499-T-G

103843575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47441764-T-C

http://identifiers.org/hco/10/GRCh38#103843768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47441964-C-A

103843768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47441964-C-T

103843816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47442139-T-C

http://identifiers.org/hco/10/GRCh38#103843834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47442186-C-A

103844297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47442740-G-A

103844317-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47442758-G-C

103844426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47442864-G-A

103844495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47442932-C-T

103844541-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47442978-G-C

103844576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47443012-C-T

http://identifiers.org/hco/10/GRCh38#103844615-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47443072-A-C

103844697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47443143-G-A

103845795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47443291-T-C

103845982-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47443451-T-G

103846148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47443599-C-T

103846383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47443779-G-A

103846652-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47444002-G-C

103846697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47444040-G-T

103846707-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47444051-G-C

103846756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47444088-G-A

103846791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47444128-G-A

103847021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47444293-A-G

103848091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47445062-G-A

103848091-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47445062-G-C

http://identifiers.org/hco/10/GRCh38#103848098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47445069-C-A

103848098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47445069-C-T

103848117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47445087-G-A

103848137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47445106-C-T

103848188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47445176-C-T

103848203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47445191-C-T

103848231-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47445210-A-T

103848237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47445216-C-T

103848285-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47445264-C-G

103848310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47445289-G-A

103848655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47445938-T-C

http://identifiers.org/hco/10/GRCh38#103848979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47446225-C-A

103848979-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47446225-C-G

103848979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47446225-C-T

103848993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47446239-G-T

103848996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47446242-G-T

103849241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47446410-C-T

103849342-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47446494-T-A

103849408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47446547-T-C

103849565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47446695-A-G

103849614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47446736-A-G

103849671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47446781-G-A

http://identifiers.org/hco/10/GRCh38#103849672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47446782-C-A

103850191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47447293-G-A

103850402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, undefined
orthologous variants: 47447513-C-T

103850446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, undefined
orthologous variants: 47447557-C-T

103851018-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47448004-T-G

103851039-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47448025-C-G

103851141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47448126-G-A

103851190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47448171-G-A

103851883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47448879-C-T

103851996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47448987-T-C

103852162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47449113-T-C

103852237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47449181-C-T

103852248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47449208-T-C

103852432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47449399-C-T

103852530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47449502-G-T

http://identifiers.org/hco/10/GRCh38#103852750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47449673-C-A

103852815-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47449729-G-C

103852815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47449729-G-T

103852906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47449816-A-G

103852932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47449840-A-G

103853829-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47450958-A-T

103854048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, undefined
orthologous variants: 47451362-C-T

http://identifiers.org/hco/10/GRCh38#103854211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#47451523-C-A

103854395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47451743-G-A

http://identifiers.org/hco/10/GRCh38#103854399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#47451747-C-A

103854506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47451865-G-A

103854668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47452029-T-C

103854786-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47452134-A-T

103854808-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47452157-C-G

103854822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: 47452171-G-T

http://identifiers.org/hco/10/GRCh38#103855073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47452427-C-A

103855268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 5 prime UTR variant
orthologous variants: 47452576-T-C

http://identifiers.org/hco/10/GRCh38#103855309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47452617-C-A

103855309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 5 prime UTR variant
orthologous variants: 47452617-C-T

103855318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 5 prime UTR variant
orthologous variants: 47452626-G-A

103855318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 5 prime UTR variant
orthologous variants: 47452626-G-T

http://identifiers.org/hco/10/GRCh38#103855364-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47452673-C-A

103855364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 5 prime UTR variant
orthologous variants: 47452673-C-T

103855426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 5 prime UTR variant
orthologous variants: 47452735-G-T

http://identifiers.org/hco/10/GRCh38#103855477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47452786-C-A

103855477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 5 prime UTR variant
orthologous variants: 47452786-C-T

103855539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 5 prime UTR variant
orthologous variants: 47452844-C-T

103855553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23664
most severe consequence: 5 prime UTR variant
orthologous variants: 47452858-C-T