31409652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: 5 prime UTR variant
orthologous variants: 130173141-G-A

31409670-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: 5 prime UTR variant
orthologous variants: 130173129-A-T

31409700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: 5 prime UTR variant
orthologous variants: 130173098-G-T

31409859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 130172936-G-A

31409859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 130172936-G-T

31409875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron variant
orthologous variants: 130172909-T-C

31409875-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron variant
orthologous variants: 130172909-T-G

http://identifiers.org/hco/1/GRCh38#31410066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130172729-C-A

31410066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron variant
orthologous variants: 130172729-C-T

31410248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 130172546-A-G

31410268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 130172527-A-G

31410269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 130172526-G-A

31410269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 130172526-G-T

31410389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 130172269-G-A

31410398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 130172260-G-A

http://identifiers.org/hco/1/GRCh38#31410418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130172240-C-A

31410645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130171830-C-T

31410875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130171639-G-T

31411652-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130170941-A-T

31413036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 130169519-G-A

31413036-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 130169519-G-C

31413036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 130169519-G-T

31413138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130169414-A-G

31413213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 130169340-G-A

31413213-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 130169340-G-C

31413213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 130169340-G-T

http://identifiers.org/hco/1/GRCh38#31413226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130169324-C-A

31413226-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 130169324-C-G

31413226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 130169324-C-T

31413229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 130169321-G-A

31413229-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 130169321-G-C

31413229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 130169321-G-T

31413415-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130169156-T-A

31413415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130169156-T-C

31413415-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130169156-T-G

http://identifiers.org/hco/1/GRCh38#31413439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130169137-C-A

31413439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130169137-C-T

31413509-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130169094-C-G

31413573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130169032-G-A

http://identifiers.org/hco/1/GRCh38#31413638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130168958-C-A

31413673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130168917-G-A

31413673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130168917-G-T

http://identifiers.org/hco/1/GRCh38#31413683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#130168909-C-A

31413683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 130168909-C-T

http://identifiers.org/hco/1/GRCh38#31413723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#130168871-C-A

31413723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 130168871-C-T

http://identifiers.org/hco/1/GRCh38#31413797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#130168802-C-A

31413797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 130168802-C-T

31413828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 130168771-C-T

http://identifiers.org/hco/1/GRCh38#31413909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#130168721-C-A

31413963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 130168670-G-A

31413963-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 130168670-G-C

http://identifiers.org/hco/1/GRCh38#31413971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#130168662-C-A

31413971-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 130168662-C-G

31413971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 130168662-C-T

31413972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 130168661-C-T

http://identifiers.org/hco/1/GRCh38#31413977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#130168656-C-A

31413977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 130168656-C-T

31414010-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 130168620-T-A

31414033-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130168582-C-G

31414033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130168582-C-T

31414077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 130168538-A-G

31414120-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130168491-A-T

31414160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130168457-T-C

31414160-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130168457-T-G

31414171-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130168446-T-G

31414180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130168437-C-T

31414307-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130168317-G-C

31414307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130168317-G-T

31414384-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130168244-T-A

31414384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130168244-T-C

31414384-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130168244-T-G

http://identifiers.org/hco/1/GRCh38#31414645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130167992-C-A

31414645-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130167992-C-G

31414700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130167941-C-T

31414723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130167917-C-T

http://identifiers.org/hco/1/GRCh38#31414831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130167818-C-A

31414831-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130167818-C-G

31414861-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130167789-A-T

http://identifiers.org/hco/1/GRCh38#31414874-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130167770-C-A

31414874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130167770-C-T

31414932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130167693-C-T

31415039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130167586-C-T

31415040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130167585-T-C

31415753-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130165148-G-C

31415753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130165148-G-T

31415934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130164993-A-G

31415991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130164957-G-A

31415991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130164957-G-T

31416014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130164936-G-A

31416014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130164936-G-T

31416025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130164927-T-C

31416101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130164867-C-T

31416490-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130164504-G-C

31417292-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 130164013-A-T

31421436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130160546-C-T

31421504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130160487-G-A

31421538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130160448-C-T

31421585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130160396-G-A

31421765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130160245-C-T

31422671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130159925-C-T

31422699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 130159898-T-C

http://identifiers.org/hco/1/GRCh38#31422832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#130159783-C-A

31423364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 130159280-C-T

31423376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 130159268-G-T

31423552-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130159148-G-C

31423603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130159117-G-T

31423643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130159074-G-A

31423667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130159050-G-A

31423679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130159038-G-A

31423679-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130159038-G-C

31423679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130159038-G-T

31423729-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 130158985-T-G

31423884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130158830-T-C

31423937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130158820-A-G

http://identifiers.org/hco/1/GRCh38#31423982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130158769-C-A

31424453-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130158447-G-C

31424453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130158447-G-T

31424537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130158374-G-A

31424537-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130158374-G-C

31424537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130158374-G-T

31424539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130158372-G-A

31424539-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130158372-G-C

31424539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130158372-G-T

31424638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130158285-T-C

31424638-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130158285-T-G

31424704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 130158221-G-A

31424740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 130158185-G-A

31424743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 130158182-T-C

http://identifiers.org/hco/1/GRCh38#31424842-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130158083-A-C

31424848-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 130158077-G-C

31424923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130158000-G-A

31424923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130158000-G-T

31424935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130157991-G-A

31424935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130157991-G-T

31425054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130157687-G-A

31425054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130157687-G-T

http://identifiers.org/hco/1/GRCh38#31425196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130157577-C-A

31425196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130157577-C-T

http://identifiers.org/hco/1/GRCh38#31425258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130157520-C-A

http://identifiers.org/hco/1/GRCh38#31425262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130157516-C-A

31425262-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130157516-C-G

31425262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130157516-C-T

31425266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130157512-G-A

31425286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130157492-G-A

31425286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130157492-G-T

31425426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130157353-G-A

31425426-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130157353-G-C

31425445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130157334-G-A

http://identifiers.org/hco/1/GRCh38#31425486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130157294-C-A

31425486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130157294-C-T

31425513-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130157261-C-G

31425513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130157261-C-T

31425599-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130157182-G-C

31425617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130157164-G-A

31425637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130157159-T-C

31425652-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130157148-T-A

31425652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130157148-T-C

31425652-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130157148-T-G

31425700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130157103-G-A

31425700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130157103-G-T

31425702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130157101-A-G

31425702-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130157101-A-T

31425745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130157022-C-T

31425959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130156790-A-G

31426135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130156690-A-G

31426240-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130156585-T-A

http://identifiers.org/hco/1/GRCh38#31426618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130154630-C-A

http://identifiers.org/hco/1/GRCh38#31426619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130154629-C-A

31426734-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 130154523-A-T

31427462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130153913-T-C

31428951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130152611-G-A

31428951-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130152611-G-C

31429047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130152513-T-C

31429076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 130152484-T-C

http://identifiers.org/hco/1/GRCh38#31429182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130152417-C-A

31429182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130152417-C-T

http://identifiers.org/hco/1/GRCh38#31429194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130152405-C-A

31429213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130152341-G-A

31429213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130152341-G-T

31429245-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130152308-T-A

31429293-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130152256-T-A

31429369-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130152181-C-G

31429369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130152181-C-T

31429391-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 130152160-C-G

31429391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 130152160-C-T

http://identifiers.org/hco/1/GRCh38#31429435-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130152122-A-C

31429454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130152103-G-A

31429462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130152095-G-A

31429522-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130152035-T-G

31429576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130151983-T-C

31432761-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130149553-G-C

31432817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130149513-G-A

31432817-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130149513-G-C

31432817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130149513-G-T

31432820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130149510-G-A

31432820-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130149510-G-C

31432820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130149510-G-T

31432835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130149495-G-A

31432835-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130149495-G-C

31432889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130149461-G-A

31432889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130149461-G-T

31432918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130149438-G-A

31432918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130149438-G-T

http://identifiers.org/hco/1/GRCh38#31432956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130149367-C-A

31432956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130149367-C-T

31432992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130149331-G-A

31433166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130149166-A-G

31433275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130149056-A-G

31433298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130149027-G-A

31433298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130149027-G-T

http://identifiers.org/hco/1/GRCh38#31433321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130149004-C-A

31433321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130149004-C-T

31433396-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130148931-G-C

http://identifiers.org/hco/1/GRCh38#31433463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130148869-C-A

31433463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130148869-C-T

31433474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130148851-G-A

31433501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130148828-G-A

31433501-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130148828-G-C

http://identifiers.org/hco/1/GRCh38#31433585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130148694-C-A

31433763-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130148414-G-C

http://identifiers.org/hco/1/GRCh38#31433940-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130147980-A-C

31433940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130147980-A-G

31433947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130147973-T-C

31433947-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130147973-T-G

31433976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130147944-G-A

31433976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130147944-G-T

http://identifiers.org/hco/1/GRCh38#31434234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130147702-C-A

31434234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130147702-C-T

http://identifiers.org/hco/1/GRCh38#31434289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130147648-C-A

31434289-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130147648-C-G

31434291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130147646-G-A

31434291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130147646-G-T

31434326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130147634-G-A

31434326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130147634-G-T

http://identifiers.org/hco/1/GRCh38#31434328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130147632-C-A

31434328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130147632-C-T

http://identifiers.org/hco/1/GRCh38#31434329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130147631-C-A

http://identifiers.org/hco/1/GRCh38#31434460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130147536-C-A

31434460-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130147536-C-G

31434460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130147536-C-T

31434630-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130147331-T-A

31434630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130147331-T-C

31434630-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130147331-T-G

http://identifiers.org/hco/1/GRCh38#31434661-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#130147300-A-C

31434661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 130147300-A-G