http://identifiers.org/hco/5/GRCh38#168291752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35871279-C-A

168291782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: 5 prime UTR variant
orthologous variants: 35871251-G-A

168291782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: 5 prime UTR variant
orthologous variants: 35871251-G-T

168291864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: 5 prime UTR variant
orthologous variants: 35871185-C-T

http://identifiers.org/hco/5/GRCh38#168291955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35871110-C-A

168291955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: 5 prime UTR variant
orthologous variants: 35871110-C-T

http://identifiers.org/hco/5/GRCh38#168292041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35871024-C-A

168292362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35870729-A-G

http://identifiers.org/hco/5/GRCh38#168292394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35870698-C-A

http://identifiers.org/hco/5/GRCh38#168292407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35870686-C-A

168292407-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35870686-C-G

168292407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35870686-C-T

http://identifiers.org/hco/5/GRCh38#168292411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35870682-C-A

168292411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35870682-C-T

http://identifiers.org/hco/5/GRCh38#168292417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35870676-C-A

168292417-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35870676-C-G

168292417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35870676-C-T

http://identifiers.org/hco/5/GRCh38#168292506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35870591-C-A

168292506-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35870591-C-G

168292682-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35870439-C-G

168292682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35870439-C-T

168293269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35869947-C-T

168293306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35869911-T-C

http://identifiers.org/hco/5/GRCh38#168293337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35869880-C-A

168293337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35869880-C-T

168293710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35869592-G-A

168294206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35868670-C-T

http://identifiers.org/hco/5/GRCh38#168294265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35868611-C-A

168294265-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35868611-C-G

168294271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35868605-G-A

168295135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35868180-C-T

168295213-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35868086-G-C

168295215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35868079-G-A

168296007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35867319-G-A

168296782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35866304-G-A

168296838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35866229-A-G

168296838-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35866229-A-T

168298439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35865200-C-T

168299572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35864349-C-T

168299626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35864296-A-G

168300447-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35863537-C-G

http://identifiers.org/hco/5/GRCh38#168300448-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35863536-A-C

168300482-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35863494-C-G

168300646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35863332-T-C

168300663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35863312-C-T

168300830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35863130-G-A

168301793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35862591-C-T

168302084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35862305-T-C

http://identifiers.org/hco/5/GRCh38#168302109-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#35862280-A-C

168302667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35861839-G-A

168302784-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35861715-G-C

168302785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35861714-A-G

http://identifiers.org/hco/5/GRCh38#168302835-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35861665-A-C

168302835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35861665-A-G

168306035-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35861081-T-A

168306430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35861019-T-C

168307125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35860633-G-A

168307142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35860616-T-C

168307359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35860411-C-T

168307390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35860379-A-G

168308187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35859954-C-T

168308346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35859521-G-T

168308389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35859479-G-A

168308398-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35859470-T-A

http://identifiers.org/hco/5/GRCh38#168308641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35859242-C-A

http://identifiers.org/hco/5/GRCh38#168309265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35858669-C-A

168309265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35858669-C-T

168309353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35858578-A-G

168313137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35855727-G-A

168313904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35855169-G-A

168314038-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35855037-C-G

168314355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35854908-G-A

168314574-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35854814-A-T

http://identifiers.org/hco/5/GRCh38#168314888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#35854593-C-A

168314888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35854593-C-T

168314983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35854478-G-A

168315002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35854451-C-T

168315066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35854390-T-C

168315291-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35854192-C-G

168315319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35854157-G-A

168315438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35854085-G-A

168315851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35853895-A-G

168315851-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35853895-A-T

168316162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35853485-G-A

168316195-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35853453-C-G

168316195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35853453-C-T

168316541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35853156-G-A

168316551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35853154-C-T

168316566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35853139-T-C

168317306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35852734-G-A

168317394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35852653-C-T

168317605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35852533-C-T

168317676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35852491-C-T

168317893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35852329-T-C

168320825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35850711-A-G

168320839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35850697-A-G

168320872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35850689-G-A

168320918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35850649-G-A

168320925-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35850642-T-A

168321013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35850589-G-A

168321013-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35850589-G-C

http://identifiers.org/hco/5/GRCh38#168321201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35850475-C-A

168322409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35849328-T-C

168322438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35849299-G-A

http://identifiers.org/hco/5/GRCh38#168322914-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35848721-A-C

168322914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35848721-A-G

168323106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35848553-T-C

http://identifiers.org/hco/5/GRCh38#168323825-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35847868-A-C

168323825-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35847868-A-T

168323830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35847864-A-G

168323885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35847807-C-T

168324139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35847533-A-G

168324678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35846943-G-A

168324740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35846890-A-G

168324757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35846864-A-G

168324799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35846822-A-G

168325432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35846213-C-T

168327141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35845034-C-T

168327563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35844692-C-T

168327958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35844307-G-A

168328109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35844158-A-G

168328300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35844003-A-G

168328464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35843882-A-G

168329032-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35843693-G-C

168329164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35843332-A-G

168329169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35843327-A-G

http://identifiers.org/hco/5/GRCh38#168329472-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35842752-A-C

168329501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35842719-G-A

168329508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35842712-A-G

168329640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35842576-A-G

168329678-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35842549-A-T

168329717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35842508-G-A

168329748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35842476-A-G

168329761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35842463-A-G

168330538-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35842008-T-A

168330643-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35841962-A-T

168330644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35841961-C-T

168330647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35841958-A-G

168330933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35841700-G-A

168330933-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35841700-G-C

168331025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35841610-G-A

168331091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35841549-C-T

168331128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35841508-T-C

168334390-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35839970-T-G

168334399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35839962-A-G

168334418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35839943-G-A

http://identifiers.org/hco/5/GRCh38#168334608-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35839785-A-C

168334614-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35839779-T-A

http://identifiers.org/hco/5/GRCh38#168334790-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35839648-A-C

168335155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35839309-A-G

168335555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35839105-G-T

168335592-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35839068-C-G

168335699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35838974-A-G

168335827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35838838-C-T

168336115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35838611-C-T

168340759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35833034-C-T

168340824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35832948-A-G

168341201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35832429-G-T

168341756-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35831846-C-G

168342284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35831378-G-A

168342308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35831354-G-A

168342362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35831304-A-G

168342426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35831237-G-A

168342560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35831131-G-A

http://identifiers.org/hco/5/GRCh38#168342670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35831030-C-A

168342757-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35830876-C-G

168342867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35830607-C-T

168342931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35830540-C-T

168342944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35830527-G-A

168342979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35830492-C-T

168343088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35830389-A-G

http://identifiers.org/hco/5/GRCh38#168343261-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35830228-A-C

168343358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35830131-A-G

168343382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35830108-A-G

168343392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35830098-A-G

168343623-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35829959-A-T

168343657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35829941-A-G

168344219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35829571-G-T

168344553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35828928-A-G

168344657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35828839-G-A

http://identifiers.org/hco/5/GRCh38#168344692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35828806-C-A

168344692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35828806-C-T

168344805-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35828741-A-T

168344806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35828740-T-C

168344865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35828667-G-A

168345478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35827945-T-C

168345557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35827869-A-G

168345646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35827816-G-A

168345833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35827671-T-C

168346196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35827199-T-C

168346345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35827060-A-G

168346756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35826600-T-C

168346777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35826579-A-G

168346777-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35826579-A-T

168346970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35826398-A-G

168346972-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35826396-A-T

168347065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35826308-T-C

168347121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35826233-C-T

168347217-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35826134-A-T

168347500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35825627-G-A

168347767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35825365-A-G

168347935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35825141-G-A

168348013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35825061-G-A

168348254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35824880-G-A

168348592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35824536-G-A

168348592-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35824536-G-C

168348725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35824388-G-A

168348818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35824307-G-A

168348819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35824306-G-A

168352971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35823654-G-T

168353137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35823484-C-T

168353388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35823261-T-C

168354812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35823062-C-T

168354856-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35823018-C-G

168354856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35823018-C-T

168354948-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35822932-C-G

168354997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35822880-A-G

http://identifiers.org/hco/5/GRCh38#168355173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35822733-C-A

168355189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35822717-G-A

168355539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35822669-C-T

168355663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35822552-G-T

168355664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35822551-T-C

168355716-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35822491-G-C

168355768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35822437-G-A

168356076-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35822226-C-G

168356076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35822226-C-T

168356095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35822208-G-A

168356110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35822178-A-G

168356158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35822113-A-G

168356309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35822000-G-A

168356309-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35822000-G-C

168357193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35821187-G-T

168357603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35818186-A-G

168357740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35818049-G-A

168357860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35817934-C-T

168360777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35815185-T-C

168360998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35814974-G-A

168361332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35814710-A-G

168361500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35814589-T-C

168361535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35814578-T-C

168361684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35814443-C-T

168362333-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35814119-T-G

http://identifiers.org/hco/5/GRCh38#168362447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35814024-C-A

168362447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35814024-C-T

168362535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35813920-A-G

168362676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35813780-A-G

168362755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35813688-A-G

168362760-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35813683-A-T

168363584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35813050-G-A

168363585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35813049-G-A

168363587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35813047-G-T

168363678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35812949-T-C

168363765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35812872-C-T

168364143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35812603-T-C

http://identifiers.org/hco/5/GRCh38#168364181-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35812566-A-C

168364448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35812304-C-T

168364449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35812303-G-A

168364773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35811818-G-T

168364891-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35811707-G-C

168365197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35811434-G-A

168365649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35810996-G-T

http://identifiers.org/hco/5/GRCh38#168365909-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#35810719-A-C

168365986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35810661-G-A

168366548-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35810190-C-G

http://identifiers.org/hco/5/GRCh38#168366556-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35810182-A-C

168366624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35810129-A-G

168366751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35810012-C-T

168366752-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35810011-C-G

168367649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35809381-G-A

168367649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35809381-G-T

168367726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35809318-T-C

168367819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35809225-A-G

168367906-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35809149-T-G

168370715-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35806800-G-C

168370741-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35806770-A-T

168370775-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35806720-C-G

168370923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35806572-A-G

168370934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35806561-T-C

168370985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35806510-C-T

168371267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35806235-C-T

168371280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35806233-G-T

http://identifiers.org/hco/5/GRCh38#168371335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35806203-C-A

168371585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35805938-C-T

168372181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35805446-G-T

168372433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35805270-A-G

168372443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35805260-A-G

168372489-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35805214-G-C

168372506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35805196-G-A

168372546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35805157-G-A

168372546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35805157-G-T

168372630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35805095-G-A

168372803-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35804822-T-G

168373044-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35804587-G-C

168373162-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35804469-C-G

168373273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35804357-T-C

168373552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35804015-G-A

168384558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35801556-T-C

168384646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35801495-A-G

168385463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35800940-G-A

168385463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35800940-G-T

168385471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35800932-G-A

168388689-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35798206-G-C

168388700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35798195-C-T

http://identifiers.org/hco/5/GRCh38#168388712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35798183-C-A

168388728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35798167-G-A

168389882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35797572-T-C

168389897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35797553-A-G

168389997-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35797445-G-C

168390378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35796173-A-G

168390568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35796034-A-G

168390916-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35795730-G-C

168391042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35795651-A-G

168391096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35795595-C-T

168391940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35794889-A-G

168392091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35794775-C-T

168392820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35794413-T-C

168392822-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35794411-T-G

http://identifiers.org/hco/5/GRCh38#168392847-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35794395-A-C

168393276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35794008-G-T

168393301-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35793983-C-G

168393336-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35793950-A-T

168393400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35793888-C-T

168393449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35793840-A-G

168393497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35793796-A-G

168393507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35793785-C-T

168393598-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35793699-G-C

168393830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35793551-G-A

http://identifiers.org/hco/5/GRCh38#168394134-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35793262-A-C

168395028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35792183-A-G

168395069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35792141-A-G

http://identifiers.org/hco/5/GRCh38#168395106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35792103-C-A

http://identifiers.org/hco/5/GRCh38#168395234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35791995-C-A

168395237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35791992-T-C

168395305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35791941-C-T

168395339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35791918-G-A

168395339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35791918-G-T

168395449-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35791800-G-T

168395676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35791445-C-T

http://identifiers.org/hco/5/GRCh38#168397592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35789648-C-A

168397624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35789611-T-C

168397717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 35789527-C-T

168397718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 35789526-T-C

http://identifiers.org/hco/5/GRCh38#168397910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35789381-C-A

http://identifiers.org/hco/5/GRCh38#168398531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35789097-C-A

168398533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35789095-G-A

168398659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35788984-A-G

168398845-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35788837-A-T

168398854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35788828-C-T

168398964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35788712-T-C

168399170-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35788547-G-C

168399221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35788496-C-T

http://identifiers.org/hco/5/GRCh38#168399385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35788379-C-A

168399385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35788379-C-T

168399393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35788371-G-A

168399393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35788371-G-T

168399406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35788352-G-T

168399830-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35788067-C-G

168401722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35787497-G-A

168401722-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35787497-G-C

168401722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35787497-G-T

http://identifiers.org/hco/5/GRCh38#168402061-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#35787228-A-C

168402327-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35786969-T-A

168402469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35786825-G-A

168402493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35786803-T-C

168402493-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35786803-T-G

168402507-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35786792-C-G

168403463-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35785331-T-G

168403610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35784907-G-A

168403768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35784747-C-T

168404150-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35784379-T-G

168404157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35784372-C-T

168404158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35784371-C-T

168404334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35784195-T-C

http://identifiers.org/hco/5/GRCh38#168404369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35784158-C-A

168404369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35784158-C-T

168404498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35784029-G-A

168404585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35783933-G-A

168404585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35783933-G-T

http://identifiers.org/hco/5/GRCh38#168404835-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35783640-A-C

168404920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35783541-C-T

168404925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35783536-T-C

168404934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35783527-A-G

168404934-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35783527-A-T

168404984-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35783481-T-G

168405138-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35783336-A-T

168405148-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35783326-G-C

168405337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35783186-G-A

168405337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35783186-G-T

168405361-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35783177-A-T

168405363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35783175-G-A

168405810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35782782-T-C

168406028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35782535-G-A

168406030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35782533-G-T

168406031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35782532-A-G

http://identifiers.org/hco/5/GRCh38#168406049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35782514-C-A

168406049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35782514-C-T

168406217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 35782384-G-A

168406354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35782262-G-A

168406357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35782259-A-G

168406389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35782217-A-G

168406416-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35782188-T-G

168406427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35782177-C-T

168408591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35780147-T-C

168408591-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35780147-T-G

168408600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35780138-C-T

168408840-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35779956-T-G

168409048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35779793-A-G

168409100-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35779742-A-T

168409106-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35779736-C-G

168409117-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35779725-T-G

168409209-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35779642-T-G

168409264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35779588-G-A

168409325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35779518-G-T

168409341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35779502-G-A

168409531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35779345-G-A

168409535-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35779341-T-G

168409552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35779324-C-T

168409595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35779283-T-C

168409602-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35779276-C-G

168409602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35779276-C-T

168409607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35779271-A-G

168409760-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35779131-G-C

http://identifiers.org/hco/5/GRCh38#168409800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#35779091-C-A

168409800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35779091-C-T

168409817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35779074-G-T

168409875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35779017-C-T

168409911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35778976-T-C

168409911-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35778976-T-G

168409985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35778898-G-A

168409998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35778885-A-G

http://identifiers.org/hco/5/GRCh38#168410104-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35778635-A-C

168410104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35778635-A-G

168410122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35778617-G-A

168410122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35778617-G-T

http://identifiers.org/hco/5/GRCh38#168410152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#35778592-C-A

168410170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 35778574-A-G

168410170-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 35778574-A-T

168410529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35777691-G-A

168410529-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35777691-G-C

168411253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35777069-G-A

http://identifiers.org/hco/5/GRCh38#168411316-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#35777005-A-C

168411382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35776940-G-A

168411469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35776852-A-G

http://identifiers.org/hco/5/GRCh38#168411565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35776765-C-A

168411565-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35776765-C-G

http://identifiers.org/hco/5/GRCh38#168411577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35776753-C-A

168411605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35776729-T-C

168411660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35776673-A-G

168411662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 35776671-C-T

168411681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35776652-T-C

168411738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35776425-G-T

168411743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35776420-G-T

http://identifiers.org/hco/5/GRCh38#168411755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35776408-C-A

168411755-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35776408-C-G

168411755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35776408-C-T

168411760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35776403-G-A

168411760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35776403-G-T

168411771-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35776392-T-A

168411778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35776386-A-G

168411784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35776380-G-T

168411790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35776374-G-A

168411790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35776374-G-T

168411819-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35776346-T-A

http://identifiers.org/hco/5/GRCh38#168411822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35776343-C-A

168411823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35776342-T-C

168411852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35776314-G-A

168411852-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35776314-G-C

168411852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35776314-G-T

168411876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35776303-G-T

168411925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35776252-T-C

168411963-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35776221-T-A

168411963-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35776221-T-G

168412002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 35776182-C-T

http://identifiers.org/hco/5/GRCh38#168412022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35776161-C-A

http://identifiers.org/hco/5/GRCh38#168412052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35776137-C-A

168412052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 35776137-C-T

168412081-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35776126-C-G

168412089-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35776118-C-G

168412089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35776118-C-T

168412103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 35776104-A-G

168412375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35775971-G-T

168413040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35775637-C-T

168413250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35775460-T-C

168413258-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35775450-C-G

168413498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35775206-G-A

168413522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35775182-G-A

168413731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35774867-C-T

168413779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35774824-G-A

168413931-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35774647-T-A

168413931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35774647-T-C

168413931-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35774647-T-G

http://identifiers.org/hco/5/GRCh38#168413949-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35774616-A-C

http://identifiers.org/hco/5/GRCh38#168413956-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35774608-A-C

168413958-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35774606-A-T

http://identifiers.org/hco/5/GRCh38#168413994-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35774573-A-C

168413994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35774573-A-G

168413994-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35774573-A-T

168414002-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35774565-T-A

168414002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35774565-T-C

168414002-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35774565-T-G

http://identifiers.org/hco/5/GRCh38#168414031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35774536-C-A

168414031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35774536-C-T

http://identifiers.org/hco/5/GRCh38#168414046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35774521-C-A

168414046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35774521-C-T

168414051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35774516-G-A

168414051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35774516-G-T

168414056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35774511-G-T

168414185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35774450-A-G

http://identifiers.org/hco/5/GRCh38#168414262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35774419-C-A

168414273-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35774399-C-G

168414288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35774384-A-G

168414314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35774356-G-A

168414442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35774221-G-A

168414442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 35774221-G-T

168414463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35774200-G-A

168414463-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35774200-G-C

168414463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 35774200-G-T

http://identifiers.org/hco/5/GRCh38#168414481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35774182-C-A

168414508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 35774155-G-T

168414599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35774064-G-A

168414599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35774064-G-T

168414675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35773954-G-A

168414675-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35773954-G-T

http://identifiers.org/hco/5/GRCh38#168414794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35773855-C-A

168414794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35773855-C-T

168414795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35773854-A-G

168414795-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35773854-A-T

http://identifiers.org/hco/5/GRCh38#168414844-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35773808-A-C

168414844-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35773808-A-T

http://identifiers.org/hco/5/GRCh38#168414881-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35773771-A-C

168414881-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35773771-A-T

http://identifiers.org/hco/5/GRCh38#168414903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35773755-C-A

168414903-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35773755-C-G

168414903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35773755-C-T

http://identifiers.org/hco/5/GRCh38#168415878-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35771200-A-C

168415878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35771200-A-G

168415958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35771119-C-T

168415972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35771105-G-T

168415977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35771099-G-A

168416035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35771056-G-A

168416035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35771056-G-T

168416036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35771055-C-T

http://identifiers.org/hco/5/GRCh38#168416059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35771032-C-A

168416059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35771032-C-T

168416117-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35770980-T-A

168416117-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35770980-T-G

168416132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35770972-A-G

168416152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35770952-A-G

168416152-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35770952-A-T

168416164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35770940-A-G

168416198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35770907-G-A

168416198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35770907-G-T

168416416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35770713-T-C

168416433-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35770696-G-C

http://identifiers.org/hco/5/GRCh38#168416497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35770633-C-A

168416497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35770633-C-T

168416620-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35770533-A-T

168417786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35769937-T-C

168417866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35769849-C-T

168417928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35769806-C-T

168417998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35769742-C-T

168418031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35769709-T-C

168418280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35769531-C-T

168418470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35769368-T-C

168418506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35769332-C-T

168418693-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35769156-T-G

168418715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35769139-T-C

168418715-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35769139-T-G

168418821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35769059-A-G

168418875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35769003-G-A

168418876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35769002-G-T

168419114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35768775-G-A

http://identifiers.org/hco/5/GRCh38#168419172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35768734-C-A

168419172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35768734-C-T

168419344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35768602-T-C

168419346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35768600-A-G

168421004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35768445-C-T

168421029-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35768422-A-T

168421336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35768121-A-G

http://identifiers.org/hco/5/GRCh38#168421913-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35767554-A-C

168421931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35767536-G-A

168422051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35767400-G-A

168422051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 35767400-G-T

http://identifiers.org/hco/5/GRCh38#168422241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35767256-C-A

168422241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35767256-C-T

168422272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35767226-A-G

168423460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35767041-A-G

168423490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35767014-T-C

168423746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: synonymous variant
orthologous variants: 35766764-C-T

168423801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: missense variant
orthologous variants: 35766709-G-A

168423801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: missense variant
orthologous variants: 35766709-G-T

168423816-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: missense variant
orthologous variants: 35766694-G-C

168423816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: missense variant
orthologous variants: 35766694-G-T

168424006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: missense variant
orthologous variants: 35766501-A-G

168424013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: synonymous variant
orthologous variants: 35766494-C-T

168424015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: missense variant
orthologous variants: 35766492-A-G

http://identifiers.org/hco/5/GRCh38#168424038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35766469-C-A

168424038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: missense variant
orthologous variants: 35766469-C-T

168424170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron variant
orthologous variants: 35766374-G-A

168424170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron variant
orthologous variants: 35766374-G-T

http://identifiers.org/hco/5/GRCh38#168424174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35766370-C-A

168424174-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron variant
orthologous variants: 35766370-C-G

168424174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron variant
orthologous variants: 35766370-C-T

http://identifiers.org/hco/5/GRCh38#168424198-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35766349-A-C

168424477-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron variant
orthologous variants: 35766073-A-T

168426025-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron variant
orthologous variants: 35765388-G-C

168426323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron variant
orthologous variants: 35765093-A-G

168426441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron variant
orthologous variants: 35764973-A-G

168426660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron variant
orthologous variants: 35764759-A-G

168426669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron variant
orthologous variants: 35764750-G-A

168426673-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron variant
orthologous variants: 35764746-C-G

168426673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron variant
orthologous variants: 35764746-C-T

168426711-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron variant
orthologous variants: 35764700-C-G

168426805-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron variant
orthologous variants: 35764596-T-A

168427039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron variant
orthologous variants: 35764365-G-A

168427065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron variant
orthologous variants: 35764344-G-A

168428148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 35761734-G-A

168428356-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron variant
orthologous variants: 35761560-A-T

168428694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron variant
orthologous variants: 35761392-T-C

168428809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35761278-G-A

168428821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35761267-G-A

168428821-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35761267-G-C

168428821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35761267-G-T

168428828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35761260-G-A

168428911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35761197-G-A

168428911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35761197-G-T

168429213-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35760960-T-A

168429998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35760270-G-T

168430026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35760242-A-G

168430030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35760238-G-A

168430030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35760238-G-T

http://identifiers.org/hco/5/GRCh38#168430043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35760225-C-A

168430046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35760222-C-T

168430108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35760035-G-T

http://identifiers.org/hco/5/GRCh38#168430115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35760028-C-A

168430117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35760026-T-C

168430162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35759983-G-A

http://identifiers.org/hco/5/GRCh38#168430242-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35759903-A-C

168430242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35759903-A-G

168430334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35759813-G-A

168430334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35759813-G-T

168430372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35759793-G-A

168430372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35759793-G-T

http://identifiers.org/hco/5/GRCh38#168430411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35759754-C-A

168431158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35758328-T-C

http://identifiers.org/hco/5/GRCh38#168431178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35758308-C-A

168431178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35758308-C-T

168431505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35758025-A-G

http://identifiers.org/hco/5/GRCh38#168431592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35757970-C-A

168431922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35757821-C-T

168432453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35757379-C-T

168432456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35757376-A-G

168432678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35757188-C-T

http://identifiers.org/hco/5/GRCh38#168432820-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35757050-A-C

http://identifiers.org/hco/5/GRCh38#168432859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35757009-C-A

168432885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35756982-T-C

168432885-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35756982-T-G

168432990-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35756878-T-G

168433034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35756835-G-A

168433394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35756521-C-T

168433400-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35756516-A-T

168434058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35756149-G-A

168434360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35755854-G-A

168434549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35755647-A-G

168434549-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35755647-A-T

168434574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35755622-G-A

168437660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35755087-C-T

168437668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35755079-C-T

168437761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35754996-A-G

168438071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35754691-G-A

168438121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35754655-A-G

168441829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35752639-A-G

168441837-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 35752631-G-C

168441842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, stop_gained
orthologous variants: 35752628-G-A

168441842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 35752628-G-T

168441843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 35752627-G-A

http://identifiers.org/hco/5/GRCh38#168441924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35752552-C-A

168441924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35752552-C-T

168441937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35752539-G-A

168441937-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35752539-G-C

168441937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35752539-G-T

http://identifiers.org/hco/5/GRCh38#168441954-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35752513-A-C

168441954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35752513-A-G

168441954-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35752513-A-T

http://identifiers.org/hco/5/GRCh38#168441988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35752479-C-A

168441988-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35752479-C-G

http://identifiers.org/hco/5/GRCh38#168442061-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35752430-C-A

http://identifiers.org/hco/5/GRCh38#168444084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35751376-C-A

168444201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35751274-C-T

168444296-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35751195-T-A

168444296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35751195-T-C

168444402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35751094-G-A

168444402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35751094-G-T

168444418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35751078-T-C

168444419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35751077-G-A

168444419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35751077-G-T

http://identifiers.org/hco/5/GRCh38#168444433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35751071-C-A

168444433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35751071-C-T

168444436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35751068-G-T

168444441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35751063-G-T

168444489-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 35751017-T-A

168444489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 35751017-T-C

168444494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 35751012-G-A

168444524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35750982-G-A

168444568-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35750938-G-C

168444623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35750906-G-A

168444623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35750906-G-T

http://identifiers.org/hco/5/GRCh38#168444624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35750905-C-A

168444624-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35750905-C-G

168444624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35750905-C-T

http://identifiers.org/hco/5/GRCh38#168444712-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35750833-A-C

168444712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35750833-A-G

168444712-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35750833-A-T

http://identifiers.org/hco/5/GRCh38#168444803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35750769-C-A

168444803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35750769-C-T

168447300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35748496-A-G

168447552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35748068-C-T

168449181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35746537-G-A

168449636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35746206-C-T

168449643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35746199-G-A

168449726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35746159-A-G

168450015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35746071-C-T

168450143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35745949-G-T

168450286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35745823-A-G

168453912-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35744359-G-C

168453969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 35744301-A-G

168453984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35744283-A-G

168454148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35744153-T-C

168454183-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35744121-G-C

168454203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35744099-G-A

http://identifiers.org/hco/5/GRCh38#168454220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35744085-C-A

http://identifiers.org/hco/5/GRCh38#168454225-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35744080-A-C

168454225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35744080-A-G

168454232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35744073-T-C

168454241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35744064-G-T

168454275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35744027-A-G

168454312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35743990-C-T

168454440-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35743884-T-A

168454653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35743837-G-A

http://identifiers.org/hco/5/GRCh38#168455204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35743352-C-A

168455204-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35743352-C-G

168455204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35743352-C-T

168455205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35743351-T-C

168455325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35743210-T-C

168455529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35743010-G-A

168455529-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35743010-G-T

168455535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35743005-G-A

168455535-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35743005-G-C

168455535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35743005-G-T

168455798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35740577-A-G

168456675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35739195-A-G

168456728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35739155-T-C

168456882-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35738987-T-G

168457783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35738339-G-A

http://identifiers.org/hco/5/GRCh38#168457924-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35738202-A-C

168457924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35738202-A-G

168458040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35738123-A-G

168460457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35735288-T-C

http://identifiers.org/hco/5/GRCh38#168460463-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35735282-A-C

168460468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35735277-T-C

168460656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35735066-C-T

http://identifiers.org/hco/5/GRCh38#168460677-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35735045-A-C

http://identifiers.org/hco/5/GRCh38#168464396-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35733108-A-C

168464474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35733034-G-A

168464474-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35733034-G-C

168464572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35732951-G-T

168464573-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35732950-T-A

168464573-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35732950-T-G

168464597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35732934-C-T

168464645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35732900-G-T

http://identifiers.org/hco/5/GRCh38#168464702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35732839-C-A

168464702-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35732839-C-G

168464702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35732839-C-T

168464736-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35732805-C-G

168464736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35732805-C-T

168464855-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35732686-C-G

168467550-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35731515-A-T

168467639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35731427-G-A

168467639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35731427-G-T

http://identifiers.org/hco/5/GRCh38#168467644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35731422-C-A

168467675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35731392-T-C

168467675-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35731392-T-G

168467682-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35731385-A-T

http://identifiers.org/hco/5/GRCh38#168467686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35731381-C-A

168467707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35731372-G-T

168467740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35731353-G-A

168467740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35731353-G-T

http://identifiers.org/hco/5/GRCh38#168467749-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35731344-A-C

168467749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35731344-A-G

http://identifiers.org/hco/5/GRCh38#168467762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35731332-C-A

168467762-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35731332-C-G

168467787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35731318-C-T

168467801-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35731304-C-G

168467801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35731304-C-T

168467894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35731205-G-T

168467993-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35731106-T-A

http://identifiers.org/hco/5/GRCh38#168468005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35731094-C-A

168468005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35731094-C-T

http://identifiers.org/hco/5/GRCh38#168468008-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35731091-A-C

http://identifiers.org/hco/5/GRCh38#168468044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35731049-C-A

168468210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35730886-G-T

http://identifiers.org/hco/5/GRCh38#168468401-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35730692-A-C

168468824-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35730224-A-T

168468858-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35730194-A-T

168468901-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35730105-G-C

168469354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35729647-G-T

http://identifiers.org/hco/5/GRCh38#168469422-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35729570-A-C

168469422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35729570-A-G

168469584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35729403-C-T

http://identifiers.org/hco/5/GRCh38#168469585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35729402-C-A

168469585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35729402-C-T

168469591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35729396-T-C

168469592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35729395-G-A

168469611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35729378-G-A

168469611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35729378-G-T

168469630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35729358-C-T

168469678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35729304-G-A

168469678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35729304-G-T

168469704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35729279-T-C

168469770-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35729216-G-C

168469770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35729216-G-T

168469916-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29435
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35729086-A-T