5274490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: 5_prime_UTR_variant, splice_region_variant
orthologous variants: 142678356-A-G

5274491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: 5_prime_UTR_variant, splice_region_variant
orthologous variants: 142678357-G-T

5274494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142678405-A-G

5274502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142678413-G-A

5274502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142678413-G-T

5274556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142678464-G-T

http://identifiers.org/hco/7/GRCh38#5274587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142678495-C-A

5274587-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142678495-C-G

5274587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142678495-C-T

http://identifiers.org/hco/7/GRCh38#5274596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142678504-C-A

5274596-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142678504-C-G

5274596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142678504-C-T

5274852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142678666-C-T

5274879-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142678687-T-A

5275014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142678789-G-A

5275272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142679233-T-C

5275280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142679243-A-G

5275351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142679310-G-A

http://identifiers.org/hco/7/GRCh38#5275392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142679350-C-A

http://identifiers.org/hco/7/GRCh38#5275447-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142679414-A-C

5275473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142679424-G-A

http://identifiers.org/hco/7/GRCh38#5275524-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142679456-A-C

5275812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142679742-C-T

5275888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142679805-A-G

5275934-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142679851-T-G

http://identifiers.org/hco/7/GRCh38#5276438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142680728-C-A

5276438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142680728-C-T

5276879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142681111-C-T

5276953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142681178-T-C

5276999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142681223-G-T

5278857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142685150-C-T

5279031-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142685315-C-G

http://identifiers.org/hco/7/GRCh38#5282119-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142687003-A-C

5282128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142687012-G-A

http://identifiers.org/hco/7/GRCh38#5282198-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142687088-A-C

5282198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142687088-A-G

5282224-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142687118-G-C

5282224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142687118-G-T

5282384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142687272-A-G

http://identifiers.org/hco/7/GRCh38#5282469-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142687344-A-C

5282469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142687344-A-G

5282469-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142687344-A-T

5282478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142687353-G-A

5282487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142687362-G-T

5282493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142687368-G-A

5282493-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142687368-G-C

5282517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142687392-A-G

http://identifiers.org/hco/7/GRCh38#5282597-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142687477-A-C

5282597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142687477-A-G

5282597-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142687477-A-T

5282639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142687529-A-G

5282642-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142687532-T-A

5282642-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142687532-T-G

5282668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142687558-G-A

5282668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142687558-G-T

5282669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142687559-G-A

5282669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142687559-G-T

5282749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142687659-A-G

5282811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142687750-G-A

5282811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142687750-G-T

5282840-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142687779-G-C

http://identifiers.org/hco/7/GRCh38#5282855-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142687797-A-C

5282855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142687797-A-G

5282855-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142687797-A-T

http://identifiers.org/hco/7/GRCh38#5282882-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142687825-A-C

5282882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142687825-A-G

5282883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142687826-G-T

5282884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142687827-G-A

http://identifiers.org/hco/7/GRCh38#5282885-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142687828-A-C

5282885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142687828-A-G

5282885-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142687828-A-T

http://identifiers.org/hco/7/GRCh38#5282917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142687861-C-A

5282917-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142687861-C-G

5282917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142687861-C-T

5282941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142687882-G-A

5282941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142687882-G-T

5283033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 142687974-C-T

http://identifiers.org/hco/7/GRCh38#5283328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142688305-C-A

5283345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142688323-C-T

5283518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142688490-G-A

http://identifiers.org/hco/7/GRCh38#5283535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142688509-C-A

5283874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142688907-T-C

5283874-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142688907-T-G

5283983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142688958-G-A

5284058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142689022-C-T

5284059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142689023-T-C

5284090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142689057-T-C

http://identifiers.org/hco/7/GRCh38#5284462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#142689270-C-A

5284469-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron_variant, undefined
orthologous variants: 142689277-C-G

5285005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142689652-C-T

5285051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142689683-C-T

5285304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142689904-G-A

5285317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142689916-G-A

5285363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142689934-G-T

5285440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142690002-G-A

5285491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142690047-G-A

5285535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142690089-A-G

5285601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142690157-T-C

http://identifiers.org/hco/7/GRCh38#5285602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142690158-C-A

5285602-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142690158-C-G

5287876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: synonymous variant
orthologous variants: 142691181-G-A

5287876-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: synonymous variant
orthologous variants: 142691181-G-C

5287876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: synonymous variant
orthologous variants: 142691181-G-T

5287921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: missense variant
orthologous variants: 142691226-G-T

5287945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: synonymous variant
orthologous variants: 142691250-G-A

5287945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: missense variant
orthologous variants: 142691250-G-T

5287966-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: synonymous variant
orthologous variants: 142691271-C-G

5287979-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: missense variant
orthologous variants: 142691284-G-C

http://identifiers.org/hco/7/GRCh38#5288019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142691312-C-A

5288019-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142691312-C-G

5288019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142691312-C-T

http://identifiers.org/hco/7/GRCh38#5288022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142691315-C-A

5288022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142691315-C-T

5288037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142691331-T-C

http://identifiers.org/hco/7/GRCh38#5288044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142691338-C-A

5288044-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142691338-C-G

5288044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142691338-C-T

http://identifiers.org/hco/7/GRCh38#5288057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142691351-C-A

5288057-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142691351-C-G

5288057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142691351-C-T

http://identifiers.org/hco/7/GRCh38#5288067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142691360-C-A

5288067-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142691360-C-G

5288067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142691360-C-T

5288090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142691383-A-G

5290577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142697535-C-T

http://identifiers.org/hco/7/GRCh38#5290602-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142697554-A-C

5290657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142697624-G-A

5290657-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142697624-G-C

5290657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142697624-G-T

http://identifiers.org/hco/7/GRCh38#5290674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142697640-C-A

5290674-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142697640-C-G

5290674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142697640-C-T

http://identifiers.org/hco/7/GRCh38#5290713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142697699-C-A

5290713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142697699-C-T

http://identifiers.org/hco/7/GRCh38#5290870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142697856-C-A

5290870-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 142697856-C-G

5290870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 142697856-C-T

http://identifiers.org/hco/7/GRCh38#5290935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142697927-C-A

5290935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142697927-C-T

5290941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142697933-G-A

5290941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142697933-G-T

5291064-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142698573-C-G

5291064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142698573-C-T

http://identifiers.org/hco/7/GRCh38#5291071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142698580-C-A

5291071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142698580-C-T

5291249-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142698765-C-G

5291252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142698768-G-A

5291252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142698768-G-T

5291256-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142698772-C-G

5291256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142698772-C-T

http://identifiers.org/hco/7/GRCh38#5291322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142698851-C-A

5291322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142698851-C-T

5291390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142698927-G-A

5291653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142699722-T-C

http://identifiers.org/hco/7/GRCh38#5291684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142699757-C-A

5291684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142699757-C-T

5294604-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142700517-C-G

5294631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142700547-G-A

5294958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142700897-G-A

5294958-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142700897-G-C

5294958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142700897-G-T

5295111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142701002-G-A

http://identifiers.org/hco/7/GRCh38#5296024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142702494-C-A

http://identifiers.org/hco/7/GRCh38#5296041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142702517-C-A

5296100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142702574-C-T

5296326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142702801-G-A

5296445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142702906-G-A

5296619-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142703037-G-C

5296802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142703194-T-C

5296802-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142703194-T-G

5296820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142703208-G-A

5296820-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142703208-G-C

5296820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142703208-G-T

5296826-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142703214-G-C

5296827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142703215-A-G

5296827-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142703215-A-T

5296884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142703274-G-A

5296884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142703274-G-T

http://identifiers.org/hco/7/GRCh38#5296900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142703296-C-A

5296900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142703296-C-T

5296907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142703307-G-A

5296907-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142703307-G-C

5296907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142703307-G-T

http://identifiers.org/hco/7/GRCh38#5296910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142703310-C-A

5296910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142703310-C-T

5296940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: synonymous variant
orthologous variants: 142703351-G-A

5296940-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: synonymous variant
orthologous variants: 142703351-G-C

5296940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: synonymous variant
orthologous variants: 142703351-G-T

http://identifiers.org/hco/7/GRCh38#5296994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142703405-C-A

5296994-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: missense variant
orthologous variants: 142703405-C-G

5296994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: synonymous variant
orthologous variants: 142703405-C-T

http://identifiers.org/hco/7/GRCh38#5297063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: missense_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#142703474-C-A

5297063-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: missense_variant, undefined
orthologous variants: 142703474-C-G

5297063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: synonymous_variant, undefined
orthologous variants: 142703474-C-T

5297207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron_variant, undefined
orthologous variants: 142703599-G-A

http://identifiers.org/hco/7/GRCh38#5298860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142704118-C-A

5298860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142704118-C-T

5299038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: synonymous variant
orthologous variants: 142704262-A-G

5299065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: synonymous variant
orthologous variants: 142704292-G-A

5299065-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: synonymous variant
orthologous variants: 142704292-G-C

5299065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: synonymous variant
orthologous variants: 142704292-G-T

5299131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142704359-G-A

5299131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142704359-G-T

http://identifiers.org/hco/7/GRCh38#5299164-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142704397-A-C

5299164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142704397-A-G

5299203-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron variant
orthologous variants: 142704422-T-G

5299260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: missense variant
orthologous variants: 142704486-G-A

5299260-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: missense variant
orthologous variants: 142704486-G-C

5299260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: missense variant
orthologous variants: 142704486-G-T

http://identifiers.org/hco/7/GRCh38#5299441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142704661-C-A

5299441-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 142704661-C-G

5299441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 142704661-C-T

5299460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 142704680-C-T

5299482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 142704685-G-A

5299482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 142704685-G-T

5299496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 142704699-T-C

5299557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 142704748-G-A

5299557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 142704748-G-T

5299562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 142704752-G-A

5299562-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 142704752-G-C

5299562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 142704752-G-T

5299660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 142704836-C-T

5299944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 142705068-T-C

5299986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 142705114-A-G

5299993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 142705121-A-G

5300047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 142705194-G-A

5300162-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 142705367-T-G

5300169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 142705374-C-T

http://identifiers.org/hco/7/GRCh38#5300218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142705433-C-A

5300218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 142705433-C-T

5300262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 142705484-G-A

5300271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 142705511-G-A

5300279-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 142705519-A-T

5300330-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 142705624-T-A

5300330-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 142705624-T-G

5300374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 142705664-G-A

5300374-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 142705664-G-C

5300375-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 142705665-T-G

5300433-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 142705723-C-G

5300433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 142705723-C-T

5300445-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 142705735-C-G

5300445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 142705735-C-T

5302707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 142706992-G-A

5302707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 142706992-G-T

http://identifiers.org/hco/7/GRCh38#5302730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142707015-C-A

5302730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 142707015-C-T

5302755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 142707053-G-A

http://identifiers.org/hco/7/GRCh38#5302760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142707058-C-A

5302760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 142707058-C-T

5302816-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 142707113-C-G

5302840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 142707137-G-A

5302840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 142707137-G-T

http://identifiers.org/hco/7/GRCh38#5302846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142707143-C-A

5302846-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 142707143-C-G

5302846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 142707143-C-T

5302875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 142707172-G-A

5302886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 142707183-G-A

5302886-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 142707183-G-C

5302886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 142707183-G-T

5302901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 142707207-G-A

5302901-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 142707207-G-C

5302901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 142707207-G-T

5302928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 142707234-G-A

5302928-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 142707234-G-C

5302928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 142707234-G-T

http://identifiers.org/hco/7/GRCh38#5302952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142707258-C-A

5302952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 142707258-C-T

http://identifiers.org/hco/7/GRCh38#5302957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142707273-C-A

http://identifiers.org/hco/7/GRCh38#5303042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142707353-C-A

5303042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 142707353-C-T

http://identifiers.org/hco/7/GRCh38#5303061-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142707372-C-A

5303061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 142707372-C-T

5303108-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 142707399-T-A

5303144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 142707427-A-G

5303155-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 142707438-T-A

5303155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 142707438-T-C

5303155-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 142707438-T-G

5303165-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 142707446-T-A

5303165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 142707446-T-C

http://identifiers.org/hco/7/GRCh38#5303220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142707498-C-A

5303220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 142707498-C-T

http://identifiers.org/hco/7/GRCh38#5303236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142707524-C-A

5303236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 142707524-C-T

5303238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 142707526-A-G

http://identifiers.org/hco/7/GRCh38#5303257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142707548-C-A

5303257-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 142707548-C-G

5303257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 142707548-C-T

5303352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 142707642-G-A

5303352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 142707642-G-T

5303425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 142707679-C-T

5303471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 142707711-A-G

5303481-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 142707739-T-A

5303481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 142707739-T-C

5303483-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 142707741-T-G

5303624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 142707870-G-A

5303624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 142707870-G-T

5303677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 142707925-G-A

5303677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 142707925-G-T

5303786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: 3 prime UTR variant
orthologous variants: 142708019-G-A

5303786-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: 3 prime UTR variant
orthologous variants: 142708019-G-C

http://identifiers.org/hco/7/GRCh38#5303854-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142708073-A-C

5303854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: 3 prime UTR variant
orthologous variants: 142708073-A-G

5303927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: 3 prime UTR variant
orthologous variants: 142708122-G-T

5303965-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: 3 prime UTR variant
orthologous variants: 142708155-T-A

5303965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: 3 prime UTR variant
orthologous variants: 142708155-T-C

5304085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: 3 prime UTR variant
orthologous variants: 142708272-G-A

5304085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: 3 prime UTR variant
orthologous variants: 142708272-G-T

5304095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: 3 prime UTR variant
orthologous variants: 142708279-G-A

5304095-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: 3 prime UTR variant
orthologous variants: 142708279-G-C

5304095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: 3 prime UTR variant
orthologous variants: 142708279-G-T

5306652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: 3 prime UTR variant
orthologous variants: 142710192-G-A

5306652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: 3 prime UTR variant
orthologous variants: 142710192-G-T

http://identifiers.org/hco/7/GRCh38#5306667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142710200-C-A

5306667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: 3 prime UTR variant
orthologous variants: 142710200-C-T

5306673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: 3 prime UTR variant
orthologous variants: 142710206-T-C

5306673-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: 3 prime UTR variant
orthologous variants: 142710206-T-G

http://identifiers.org/hco/7/GRCh38#5306677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142710210-C-A

5306677-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: 3 prime UTR variant
orthologous variants: 142710210-C-G

5306677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: 3 prime UTR variant
orthologous variants: 142710210-C-T

http://identifiers.org/hco/7/GRCh38#5306679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142710212-C-A

5306679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: 3 prime UTR variant
orthologous variants: 142710212-C-T

5306740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23097
most severe consequence: 3 prime UTR variant
orthologous variants: 142710290-C-T