114120989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56776038-C-T

114121285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56776247-T-C

114121387-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56776361-T-G

114121478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56776450-T-C

http://identifiers.org/hco/10/GRCh38#114122106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56776679-C-A

114122106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56776679-C-T

114122120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56776691-T-C

114122120-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56776691-T-G

114122195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56776747-G-A

http://identifiers.org/hco/10/GRCh38#114122368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56776886-C-A

114122368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56776886-C-T

114122928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56777394-A-G

114122935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56777401-A-G

114123074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56777542-A-G

http://identifiers.org/hco/10/GRCh38#114123086-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56777554-A-C

114123180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56777650-A-G

114123425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56777872-G-A

114123425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56777872-G-T

114123705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56778260-A-G

114123771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56778329-T-C

114123783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56778340-G-T

114123807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56778359-T-C

114123812-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56778364-T-G

114123825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56778377-T-C

http://identifiers.org/hco/10/GRCh38#114124489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56778657-C-A

114124567-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56778719-G-C

114124567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56778719-G-T

114124732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56778998-G-T

114124795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56779062-T-C

114124970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56779236-A-G

114125385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56779619-G-A

114125639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56779995-C-T

114125811-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56780298-T-G

http://identifiers.org/hco/10/GRCh38#114125835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56780322-C-A

114125835-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56780322-C-G

114125835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56780322-C-T

114125861-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56780348-G-C

114125862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56780349-T-C

114126159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56780640-G-T

114126171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56780652-G-A

114126171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56780652-G-T

http://identifiers.org/hco/10/GRCh38#114126219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56780713-C-A

114127272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56781449-G-A

http://identifiers.org/hco/10/GRCh38#114127718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56781976-C-A

114127718-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56781976-C-G

114127793-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56782035-A-T

114128031-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56782315-T-A

114128095-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56782394-G-C

http://identifiers.org/hco/10/GRCh38#114128168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56782456-C-A

http://identifiers.org/hco/10/GRCh38#114128350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56782649-C-A

114129843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56783478-A-G

114129922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56783553-G-A

114129936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56783567-A-G

114129936-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56783567-A-T

114130095-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56783753-T-A

114130095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56783753-T-C

114130095-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56783753-T-G

114130102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56783760-G-A

114130102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56783760-G-T

114130318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56784161-G-A

114130318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56784161-G-T

http://identifiers.org/hco/10/GRCh38#114130501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56784316-C-A

114131202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56785931-A-G

114131264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56785993-T-C

114131342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 56786071-T-C

114131342-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 56786071-T-G

114131458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56786191-T-C

114131474-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56786207-C-G

114131474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56786207-C-T

114131745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56786383-G-A

114131919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56786989-T-C

114131920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56786990-T-C

114131948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56787018-T-C

114131977-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56787047-A-T

114131984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56787054-C-T

114132004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56787074-T-C

114132040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56787110-T-C

114132052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56787122-A-G

114132236-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56787310-A-T

http://identifiers.org/hco/10/GRCh38#114132317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56787386-C-A

114132320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56787389-A-G

http://identifiers.org/hco/10/GRCh38#114132327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56787396-C-A

114132327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56787396-C-T

http://identifiers.org/hco/10/GRCh38#114132627-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56787632-A-C

114134121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56787912-G-A

114134486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56788147-G-A

114134486-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56788147-G-C

114134710-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56788343-G-C

114134738-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56788376-A-T

114135023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56788606-T-C

114135023-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56788606-T-G

114135133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56788715-G-A

114135133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56788715-G-T

114135289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56788783-A-G

114135366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56788858-T-C

http://identifiers.org/hco/10/GRCh38#114135810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56789274-C-A

114135877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56789331-A-G

114136005-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56789446-A-T

114136078-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56789521-T-A

114136090-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56789531-A-T

114136128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56789572-T-C

114137298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 56790429-G-T

http://identifiers.org/hco/10/GRCh38#114137328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56790460-C-A

114137328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56790460-C-T

http://identifiers.org/hco/10/GRCh38#114141416-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56793223-A-C

114141782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56793408-T-C

114141801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56793427-G-A

114141819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56793447-G-T

114143440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56794219-T-C

114143588-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56794325-G-C

114144051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56794954-A-G

114144222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56795151-T-C

http://identifiers.org/hco/10/GRCh38#114144290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56795220-C-A

114144290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56795220-C-T

114144389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56795312-T-C

114144389-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56795312-T-G

114144411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56795334-G-T

114144595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56795496-T-C

114144595-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56795496-T-G

114144654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56795548-A-G

http://identifiers.org/hco/10/GRCh38#114144752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56795635-C-A

114144752-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56795635-C-G

114144752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56795635-C-T

114144756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56795639-T-C

114144821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56795704-T-C

114145051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56795846-G-A

114145107-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56795904-T-A

114145207-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56796111-C-G

114145207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56796111-C-T

114145286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56796187-T-C

114145290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56796190-T-C

114145359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56796273-T-C

114145406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56796303-T-C

114145416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56796308-A-G

114145437-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56796329-T-A

114145448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56796338-G-T

114145457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56796346-A-G

114145774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56796636-T-C

114145797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56796655-T-C

http://identifiers.org/hco/10/GRCh38#114145883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56796733-C-A

114146138-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56796905-C-G

http://identifiers.org/hco/10/GRCh38#114146139-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56796906-A-C

http://identifiers.org/hco/10/GRCh38#114150600-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56797226-A-C

114151289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56797835-A-G

114157638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56798755-G-A

114157742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56798824-G-A

114157742-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56798824-G-C

114157742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56798824-G-T

http://identifiers.org/hco/10/GRCh38#114160593-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56799723-A-C

114160593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56799723-A-G

http://identifiers.org/hco/10/GRCh38#114160831-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56799926-A-C

114160889-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56799984-T-G

114160940-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56800026-A-T

114160943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56800029-A-G

114160952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56800038-T-C

114160996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56800061-T-C

114161076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56800117-C-T

114161078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56800119-G-A

114162257-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56801202-T-G

114162311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56801218-T-C

114162715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56801505-T-C

114162715-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56801505-T-G

114162719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56801509-T-C

114162862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56801655-T-C

114162865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56801658-G-A

114162877-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56801670-G-C

114162887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56801680-G-A

114162887-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56801680-G-C

114162891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56801684-T-C

http://identifiers.org/hco/10/GRCh38#114163377-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56802157-C-A

114163377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56802157-C-T

114163757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56802419-T-C

114164039-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56802642-C-G

114165004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56803591-G-T

114165025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56803612-C-T

114165178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56803755-T-C

114165217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56803807-T-C

114165224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56803814-T-C

http://identifiers.org/hco/10/GRCh38#114166294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#56805522-C-A

114166299-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 56805527-T-G

114166694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56805872-G-A

114166801-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56805973-T-G

114166913-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56806079-T-G

114167015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56806180-G-T

114167431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56806301-G-A

114167479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56806360-C-T

114167536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56806418-G-A

114167536-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56806418-G-C

http://identifiers.org/hco/10/GRCh38#114168149-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56806710-A-C

114169571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56807409-A-G

114169592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56807427-T-C

114169630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56807472-T-C

114169840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56807684-T-C

114171583-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56808441-T-A

114171583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56808441-T-C

114172616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56809430-C-T

114173017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56809800-A-G

114173260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56810015-T-C

114173336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56810091-T-C

114173337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56810092-G-T

http://identifiers.org/hco/10/GRCh38#114173658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56810238-C-A

114173679-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 56810259-T-A

http://identifiers.org/hco/10/GRCh38#114173967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56810381-C-A

114173967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56810381-C-T

114173990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 56810395-C-T

http://identifiers.org/hco/10/GRCh38#114174140-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#56810545-A-C

114174159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 56810566-G-A

114174159-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 56810566-G-C

114174159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 56810566-G-T

114174168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24349
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 56810575-C-T