53054664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78029613-T-C

53054789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78029505-A-G

53054795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78029499-G-T

53054832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78029462-C-T

53054892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78029418-G-A

53054892-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78029418-G-C

53055305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78029192-T-C

53055384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78029119-T-C

53055475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78029029-G-A

53055549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78028955-C-T

53055558-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78028951-G-C

53056225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78028539-G-A

53056417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78028373-A-G

53056425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78028365-A-G

http://identifiers.org/hco/6/GRCh38#53056525-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78028303-A-C

53057429-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78026871-T-G

53057577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78026834-T-C

53057577-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78026834-T-G

53057612-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78026805-T-A

53057612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78026805-T-C

53057815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78025932-T-C

53057878-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78025881-C-G

53057878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78025881-C-T

53058150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78025701-T-C

53058287-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78025576-T-G

53058290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78025573-G-A

53058332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78025535-A-G

http://identifiers.org/hco/6/GRCh38#53058454-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78025270-A-C

53058527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78025197-C-T

53058565-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78025163-C-G

53058565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78025163-C-T

53058588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78025144-A-G

53058761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78024154-C-T

53058795-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78023607-A-T

53059134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78023284-C-T

53059150-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78023268-A-T

53059153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78023265-C-T

53059159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78023259-T-C

53059634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78022807-C-T

53059731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78022549-A-G

53059744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78022536-C-T

53060023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78022279-T-C

53060056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78022265-T-C

53060170-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78022137-G-C

53060377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78021940-T-C

53060490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78021795-T-C

53060837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78021461-G-A

53061017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78021302-T-C

53061337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78020971-G-A

53061466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78020836-A-G

53061558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78020774-G-A

53061558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78020774-G-T

53062067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron variant
orthologous variants: 78020309-T-C

http://identifiers.org/hco/6/GRCh38#53062644-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78019590-A-C

53062644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron variant
orthologous variants: 78019590-A-G

53062662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron variant
orthologous variants: 78019572-T-C

53062771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron variant
orthologous variants: 78019430-A-G

53062968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron variant
orthologous variants: 78019180-T-C

53062999-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron variant
orthologous variants: 78019168-C-G

53063327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron variant
orthologous variants: 78018813-T-C

53063467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron variant
orthologous variants: 78018659-G-T

http://identifiers.org/hco/6/GRCh38#53063571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78018422-C-A

53064892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron variant
orthologous variants: 78016375-T-C

http://identifiers.org/hco/6/GRCh38#53064898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78016369-C-A

53064961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron variant
orthologous variants: 78016306-C-T

53064964-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron variant
orthologous variants: 78016299-C-G

http://identifiers.org/hco/6/GRCh38#53064973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78016290-C-A

53064973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron variant
orthologous variants: 78016290-C-T

53065053-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 78016237-G-C

http://identifiers.org/hco/6/GRCh38#53065253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78016063-C-A

53065253-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron variant
orthologous variants: 78016063-C-G

53065253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron variant
orthologous variants: 78016063-C-T

53065260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron variant
orthologous variants: 78016056-T-C

http://identifiers.org/hco/6/GRCh38#53065268-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78016050-A-C

53065268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron variant
orthologous variants: 78016050-A-G

http://identifiers.org/hco/6/GRCh38#53065279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78016048-C-A

53065279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron variant
orthologous variants: 78016048-C-T

http://identifiers.org/hco/6/GRCh38#53065291-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78016036-A-C

53065291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron variant
orthologous variants: 78016036-A-G

53065291-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron variant
orthologous variants: 78016036-A-T

53065324-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron variant
orthologous variants: 78016007-C-G

http://identifiers.org/hco/6/GRCh38#53065330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78016001-C-A

http://identifiers.org/hco/6/GRCh38#53065361-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78015989-A-C

53065361-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron variant
orthologous variants: 78015989-A-T

53065387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron variant
orthologous variants: 78015953-C-T

http://identifiers.org/hco/6/GRCh38#53065396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78015944-C-A

53065396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron variant
orthologous variants: 78015944-C-T

53065473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78015867-G-A

53065486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78015854-T-C

http://identifiers.org/hco/6/GRCh38#53065512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78015828-C-A

53065512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78015828-C-T

53065573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78015775-G-A

53065573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78015775-G-T

53065620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 78015728-G-A

53065620-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 78015728-G-C

53065620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 78015728-G-T

53065629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 78015719-T-C

53065629-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 78015719-T-G

53065639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 78015709-G-A

53065639-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 78015709-G-C

53065639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 78015709-G-T

http://identifiers.org/hco/6/GRCh38#53065781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78015582-C-A

53065781-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78015582-C-G

53065781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78015582-C-T

53065945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78015556-A-G

53066052-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78015517-G-C

53066052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78015517-G-T

53066164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78015441-G-A

53066164-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78015441-G-C

53066184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78015421-G-A

53066184-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78015421-G-C

53066184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78015421-G-T

53066308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78015312-C-T

53066366-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78015229-G-C

53066841-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78014822-G-C

53067079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78014697-T-C

http://identifiers.org/hco/6/GRCh38#53067209-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78014572-A-C

53067888-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78012978-C-G

53067888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78012978-C-T

53067961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78012907-A-G

53068032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron variant
orthologous variants: 78012837-A-G

53068040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron variant
orthologous variants: 78012829-A-G

53068090-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron variant
orthologous variants: 78012784-T-A

53068090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron variant
orthologous variants: 78012784-T-C

53068090-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron variant
orthologous variants: 78012784-T-G

http://identifiers.org/hco/6/GRCh38#53068172-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78012651-A-C

53068441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron variant
orthologous variants: 78012295-C-T

53068446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron variant
orthologous variants: 78012289-A-G

53068450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron variant
orthologous variants: 78012285-C-T

53068451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron variant
orthologous variants: 78012284-G-A

53068451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron variant
orthologous variants: 78012284-G-T

53071063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 78011628-G-A

53071063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 78011628-G-T

53071205-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78011505-T-G

53071351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78010704-G-A

53071507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78010571-A-G

53071728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78010339-A-G

http://identifiers.org/hco/6/GRCh38#53072264-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78009966-A-C

53072852-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78009656-C-G

53072975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78009643-G-A

http://identifiers.org/hco/6/GRCh38#53073353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78009141-C-A

53073353-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78009141-C-G

53073353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78009141-C-T

53073404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78009026-G-A

53073557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 78008890-G-A

53073557-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 78008890-G-C

http://identifiers.org/hco/6/GRCh38#53073662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78008786-C-A

53073662-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78008786-C-G

53073714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78008746-G-A

53073714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78008746-G-T

53073721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78008739-T-C

53073737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78008723-G-A

53076347-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78007401-T-A

53076347-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78007401-T-G

53076423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78007202-T-C

53076514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 78007097-A-G

53076514-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 78007097-A-T

53076890-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78006882-A-T

53077080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78006709-A-G

53077134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78006659-A-G

53077660-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78006356-C-G

53077763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78006256-C-T

53077829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78006198-G-A

53078632-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78005872-T-G

53078647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78005857-A-G

53078743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78005776-A-G

53078873-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 78005651-G-C

53078900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 78005624-T-C

53078900-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 78005624-T-G

53079889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78004662-C-T

53080626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78003604-G-T

http://identifiers.org/hco/6/GRCh38#53080829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78003418-C-A

53080863-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78003384-A-T

53080934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78003314-G-T

http://identifiers.org/hco/6/GRCh38#53080969-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78003277-A-C

53080969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 78003277-A-G

53080969-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 78003277-A-T

53080985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 78003261-A-G

53081172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78003091-A-G

53081172-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78003091-A-T

53082145-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78002825-A-T

53082328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78002687-C-T

53082376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78002643-G-T

53082457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78002580-T-C

53082457-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78002580-T-G

http://identifiers.org/hco/6/GRCh38#53082691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78002364-C-A

53082702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78002353-A-G

53082742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78002288-T-C

53082890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78002146-G-A

53082936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78002110-T-C

53083212-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78001928-C-G

53083212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78001928-C-T

http://identifiers.org/hco/6/GRCh38#53091808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77995385-C-A

53091808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77995385-C-T

53091858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77995356-C-T

53091868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77995346-G-T

53091893-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77995327-T-A

53091923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77995312-T-C

http://identifiers.org/hco/6/GRCh38#53091962-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77995275-A-C

53091962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77995275-A-G

53091962-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77995275-A-T

http://identifiers.org/hco/6/GRCh38#53091963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77995274-C-A

53091963-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77995274-C-G

53091963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77995274-C-T

http://identifiers.org/hco/6/GRCh38#53092015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77995229-C-A

53092015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77995229-C-T

http://identifiers.org/hco/6/GRCh38#53092059-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77995193-A-C

53092059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77995193-A-G

53092059-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77995193-A-T

53092218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77995079-G-A

53092218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77995079-G-T

http://identifiers.org/hco/6/GRCh38#53092256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77995059-C-A

53092385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77994918-T-C

53092390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77994913-G-A

53092439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77994858-A-G

53092445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77994852-C-T

53092490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77994807-G-A

53092532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77994765-C-T

53092538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77994759-C-T

53092557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77994740-A-G

53092617-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77994680-T-A

53092617-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77994680-T-G

53092652-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77994644-T-A

53092652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77994644-T-C

53092681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77994615-G-T

53092684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77994612-G-T

53092834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77994444-T-C

53092855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77994423-A-G

53092922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77994364-A-G

53092929-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77994357-T-A

53092929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77994357-T-C

http://identifiers.org/hco/6/GRCh38#53092960-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77994325-A-C

53092960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77994325-A-G

53092960-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77994325-A-T

53092962-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77994323-T-A

53092962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77994323-T-C

53093009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77994277-G-T

53093010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77994276-G-A

53093010-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77994276-G-T

53093108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77994191-T-C

http://identifiers.org/hco/6/GRCh38#53093225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77994060-C-A

http://identifiers.org/hco/6/GRCh38#53093277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77994007-C-A

53093277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77994007-C-T

53093367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77993934-G-T

http://identifiers.org/hco/6/GRCh38#53093387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77993914-C-A

53093394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77993907-A-G

53093635-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77993498-A-T

53093857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77993304-T-C

53094069-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77993104-T-G

53094083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77993101-T-C

53094088-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77993096-T-A

53094088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77993096-T-C

53094088-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77993096-T-G

53094267-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77992976-T-A

53094632-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77992652-A-T

53094670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77992631-T-C

http://identifiers.org/hco/6/GRCh38#53094698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77992604-C-A

53094737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 77992570-T-C

53094740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 77992567-T-C

53094747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 77992560-G-A

53094811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 77992523-T-C

53094819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 77992515-A-G

53094819-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 77992515-A-T

53095382-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77992041-G-C

http://identifiers.org/hco/6/GRCh38#53095444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77991986-C-A

53095445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77991985-A-G

53096474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77990926-C-T

53096503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77990899-T-C

53097726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77989364-A-G

53098048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 77989080-A-G

53098049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 77989079-G-A

53098049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 77989079-G-T

53098163-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: 3_prime_UTR_variant, splice_region_variant, synonymous_variant
orthologous variants: 77988972-T-A

53098163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: 3_prime_UTR_variant, splice_region_variant, synonymous_variant
orthologous variants: 77988972-T-C

53098189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: 3 prime UTR variant
orthologous variants: 77988948-T-C

53098285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: 3 prime UTR variant
orthologous variants: 77988860-T-C

http://identifiers.org/hco/6/GRCh38#53098430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77988721-C-A

53098486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: 3 prime UTR variant
orthologous variants: 77988670-G-T

53098488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: 3 prime UTR variant
orthologous variants: 77988668-C-T

53098740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13588
most severe consequence: 3 prime UTR variant
orthologous variants: 77988569-C-T