http://identifiers.org/hco/1/GRCh38#30732557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130663370-C-A

http://identifiers.org/hco/1/GRCh38#30732588-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130663318-A-C

30732588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 130663318-A-G

http://identifiers.org/hco/1/GRCh38#30733283-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130662349-A-C

30733313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 130662323-A-G

30733345-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 130662296-T-G

30733355-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 130662275-G-C

30733367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 130662255-T-C

30733389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 130662242-G-T

http://identifiers.org/hco/1/GRCh38#30733430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130662201-C-A

30733525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: 3 prime UTR variant
orthologous variants: 130662132-A-G

30733525-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: 3 prime UTR variant
orthologous variants: 130662132-A-T

30733538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: 3 prime UTR variant
orthologous variants: 130662117-T-C

30733614-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: 3 prime UTR variant
orthologous variants: 130662046-G-C

http://identifiers.org/hco/1/GRCh38#30733615-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130662045-A-C

30733643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: 3 prime UTR variant
orthologous variants: 130662020-T-C

30733667-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: 3 prime UTR variant
orthologous variants: 130662001-G-C

http://identifiers.org/hco/1/GRCh38#30733670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130661998-C-A

30733680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: 3 prime UTR variant
orthologous variants: 130661988-G-A

30733680-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: 3 prime UTR variant
orthologous variants: 130661988-G-T

30733683-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: 3 prime UTR variant
orthologous variants: 130661986-C-G

30733683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: 3 prime UTR variant
orthologous variants: 130661986-C-T

http://identifiers.org/hco/1/GRCh38#30733691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130661978-C-A

30733691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: 3 prime UTR variant
orthologous variants: 130661978-C-T

http://identifiers.org/hco/1/GRCh38#30733785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130661903-C-A

30733785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: 3 prime UTR variant
orthologous variants: 130661903-C-T

30733829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: undefined
orthologous variants: 130661858-C-T

30733895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 130661792-T-C

http://identifiers.org/hco/1/GRCh38#30733962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130661730-C-A

30733962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130661730-C-T

30733982-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130661709-T-A

30733982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130661709-T-C

http://identifiers.org/hco/1/GRCh38#30733996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130661693-C-A

30733996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130661693-C-T

30734231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130661524-C-T

30734248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130661499-G-A

30734273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130661474-C-T

30734423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130661340-T-C

30734528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130661255-T-C

30734565-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130661218-C-G

30734565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130661218-C-T

http://identifiers.org/hco/1/GRCh38#30734680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130661100-C-A

30734697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130661083-A-G

30735106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130659486-G-A

30735106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130659486-G-T

30735144-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130659448-G-C

30735144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130659448-G-T

http://identifiers.org/hco/1/GRCh38#30735229-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130659362-A-C

30735229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 130659362-A-G

http://identifiers.org/hco/1/GRCh38#30735312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130659280-C-A

30735312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130659280-C-T

30735313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130659279-A-G

30735479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130659111-T-C

30737313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130658473-T-C

30737316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130658470-G-T

30737424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130658352-C-T

http://identifiers.org/hco/1/GRCh38#30737435-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130658341-A-C

http://identifiers.org/hco/1/GRCh38#30737456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130658320-C-A

30737456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130658320-C-T

30737464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130658312-A-G

30737502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130658280-G-A

30737502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130658280-G-T

30737538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130658244-G-A

30737538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130658244-G-T

30737568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130658213-A-G

30737579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130658202-A-G

30737585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130658196-A-G

30737666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 130658113-T-C

http://identifiers.org/hco/1/GRCh38#30737674-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130658105-A-C

30737674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 130658105-A-G

30737674-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 130658105-A-T

30737683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 130658096-T-C

30737705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 130658074-A-G

30737727-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130658054-T-A

30737762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130657953-A-G

http://identifiers.org/hco/1/GRCh38#30737767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130657948-C-A

30737767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130657948-C-T

http://identifiers.org/hco/1/GRCh38#30737815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130657897-C-A

30737815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130657897-C-T

http://identifiers.org/hco/1/GRCh38#30737822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130657895-C-A

30737822-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130657895-C-G

30737822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130657895-C-T

30737826-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130657891-T-A

30737826-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130657891-T-G

http://identifiers.org/hco/1/GRCh38#30737838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130657879-C-A

30737838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130657879-C-T

30737839-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130657878-A-T

30738463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130657232-G-A

30738636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130657087-A-G

30738789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130656988-G-A

30738789-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130656988-G-C

30738789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130656988-G-T

30738864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130656925-A-G

30738864-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130656925-A-T

30739101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130656697-G-A

30739101-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130656697-G-T

30739129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130656686-A-G

http://identifiers.org/hco/1/GRCh38#30739130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130656685-C-A

30739179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 130656639-C-T

http://identifiers.org/hco/1/GRCh38#30739291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130656532-C-A

30739291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130656532-C-T

30739311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130656513-T-C

30739327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130656497-T-C

30739433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130656390-C-T

30739815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 130656065-G-A

30739815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 130656065-G-T

30739837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 130656046-T-C

http://identifiers.org/hco/1/GRCh38#30739863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130656020-C-A

30739863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 130656020-C-T

http://identifiers.org/hco/1/GRCh38#30739879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130656004-C-A

30739879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 130656004-C-T

http://identifiers.org/hco/1/GRCh38#30740015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130655872-C-A

30740015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130655872-C-T

30740034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130655839-C-T

http://identifiers.org/hco/1/GRCh38#30740046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130655819-C-A

30740046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130655819-C-T

http://identifiers.org/hco/1/GRCh38#30740049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130655816-C-A

30740049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130655816-C-T

30740328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130655114-G-A

http://identifiers.org/hco/1/GRCh38#30740334-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130655108-A-C

30740334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130655108-A-G

30740361-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130655077-C-G

30740691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130654837-T-C

30740797-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130654745-G-C

30741209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130654412-G-T

30741450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 130654267-G-A

30741585-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130654221-A-T

30741591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130654215-T-C

30741591-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130654215-T-G

30741613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130654186-G-T

http://identifiers.org/hco/1/GRCh38#30741650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130654146-C-A

30741650-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 130654146-C-G

30741650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 130654146-C-T

http://identifiers.org/hco/1/GRCh38#30741763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130654060-C-A

30741763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130654060-C-T

30741766-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130654057-C-G

30741766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130654057-C-T

http://identifiers.org/hco/1/GRCh38#30741886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130653988-C-A

http://identifiers.org/hco/1/GRCh38#30741959-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130653915-A-C

30741959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130653915-A-G

30741959-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130653915-A-T

30741965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130653909-G-A

30741965-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130653909-G-T

30742038-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130653808-T-G

http://identifiers.org/hco/1/GRCh38#30742113-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130653741-A-C

30742113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130653741-A-G

30742151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130653738-A-G

30742152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130653737-G-A

30742152-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130653737-G-C

30742152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130653737-G-T

30742295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130653650-G-A

30742295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130653650-G-T

30742301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130653644-A-G

http://identifiers.org/hco/1/GRCh38#30742306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130653632-C-A

30742307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130653631-T-C

30742358-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130653593-A-T

http://identifiers.org/hco/1/GRCh38#30742380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130653567-C-A

30742380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130653567-C-T

30742381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130653566-T-C

30742381-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130653566-T-G

http://identifiers.org/hco/1/GRCh38#30742399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130653548-C-A

30742399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130653548-C-T

30742409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130653545-C-T

30742642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130653369-G-A

30742642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130653369-G-T

30743128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130652895-A-G

30743459-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130652610-C-G

30743528-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130652547-C-G

30743600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130652476-A-G

30743834-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130652266-T-A

30743881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130652224-G-A

30743907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130652198-G-A

30743951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130652170-C-T

30744045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130652079-T-C

30744073-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130652053-C-G

30744236-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130651922-A-T

30744625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130651767-C-T

30744712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130651674-G-A

30744712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130651674-G-T

30744784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130651610-G-T

30744833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130651562-G-A

30748393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130648743-C-T

30748450-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130648684-T-A

http://identifiers.org/hco/1/GRCh38#30748481-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130648649-A-C

30748553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130648578-C-T

30748688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130648446-C-T

30750484-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130646022-C-G

30750484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130646022-C-T

30750537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130645978-A-G

30750608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130645911-T-C

30750790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130645723-G-A

30750821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 130645707-T-C

30750845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 130645683-C-T

30751039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130645512-A-G

30751052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130645499-A-G

30751293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130645255-C-T

30751389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130645173-T-C

http://identifiers.org/hco/1/GRCh38#30755671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130642501-C-A

30756484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 130641676-C-T

30756669-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130641524-C-G

30756764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 130641442-G-A

30756764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 130641442-G-T

30756935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130641273-G-A

30757017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 130641208-C-T

30757019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 130641206-A-G

http://identifiers.org/hco/1/GRCh38#30757140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130641099-C-A

30757227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130641029-G-A

30757227-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130641029-G-C

30757286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130640984-T-C

http://identifiers.org/hco/1/GRCh38#30757339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130640947-C-A

30757339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130640947-C-T

30757522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130640887-G-A

30757522-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130640887-G-C

30757522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130640887-G-T

http://identifiers.org/hco/1/GRCh38#30757606-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130640811-A-C

30757606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130640811-A-G

http://identifiers.org/hco/1/GRCh38#30757615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130640802-C-A

30757615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130640802-C-T

http://identifiers.org/hco/1/GRCh38#30757648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130640754-C-A

30757648-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130640754-C-G

30757648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130640754-C-T