86214232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: 3 prime UTR variant
orthologous variants: 19841724-G-A

86214417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 19841567-T-C

86214446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 19841538-A-G

86214456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 19841528-T-C

86214515-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 19841469-T-A

86214539-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 19841445-A-T

86214661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron variant
orthologous variants: 19841324-G-A

86214661-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron variant
orthologous variants: 19841324-G-T

86214663-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron variant
orthologous variants: 19841322-T-A

86214663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron variant
orthologous variants: 19841322-T-C

86214742-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron variant
orthologous variants: 19841246-T-A

86214742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron variant
orthologous variants: 19841246-T-C

86214757-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron variant
orthologous variants: 19841231-T-A

86214757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron variant
orthologous variants: 19841231-T-C

86214757-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron variant
orthologous variants: 19841231-T-G

86214821-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron variant
orthologous variants: 19841171-A-T

86214926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron variant
orthologous variants: 19841063-T-C

86215126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron variant
orthologous variants: 19840869-C-T

86215767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron variant
orthologous variants: 19840449-A-G

86215770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron variant
orthologous variants: 19840446-G-A

86215790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron variant
orthologous variants: 19840427-T-C

86215820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron variant
orthologous variants: 19840398-G-A

86215840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron variant
orthologous variants: 19840367-C-T

86215958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron variant
orthologous variants: 19840257-T-C

86216067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron variant
orthologous variants: 19840055-G-T

86216293-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron variant
orthologous variants: 19839840-T-G

http://identifiers.org/hco/8/GRCh38#86216304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19839829-C-A

86216523-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron variant
orthologous variants: 19839637-A-T

86217643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 19839408-G-A

86217643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 19839408-G-T

86217648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 19839403-G-A

86217648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 19839403-G-T

86217786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 19839265-G-A

86217860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19839191-A-G

86217860-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19839191-A-T

http://identifiers.org/hco/8/GRCh38#86217924-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19839126-A-C

86217924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19839126-A-G

86218302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19838770-T-C

86218373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19838721-C-T

86218452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19838642-G-A

86218462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19838632-C-T

86218497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19838596-G-A

http://identifiers.org/hco/8/GRCh38#86218965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19831522-C-A

86219006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19831481-T-C

86219039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19831449-T-C

86219163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19830356-T-C

86219450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19830099-T-C

86219536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19830002-C-T

86219605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19829932-T-C

86220204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19828427-A-G

86220215-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19828417-T-A

http://identifiers.org/hco/8/GRCh38#86220262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19828372-C-A

86220351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19828298-C-T

86220384-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19828265-A-T

86220387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19828262-T-C

http://identifiers.org/hco/8/GRCh38#86221010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19827544-C-A

86221266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19827150-A-G

86221268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19827148-T-C

http://identifiers.org/hco/8/GRCh38#86221280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19827137-C-A

86221337-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19827084-T-G

86221361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19827060-T-C

86221402-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19827018-T-G

86222694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19824282-G-A

86222694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19824282-G-T

http://identifiers.org/hco/8/GRCh38#86222755-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19824236-A-C

86222908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19824119-G-A

86222908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19824119-G-T

86222946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19824080-A-G

86222947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19824079-T-C

86223010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 19824015-T-C

86223010-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 19824015-T-G

http://identifiers.org/hco/8/GRCh38#86223034-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19823991-A-C

86223795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19823799-A-G

86223933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19823732-A-G

86224129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19823557-G-A

86224195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19823495-C-T

86224206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19823484-G-T

http://identifiers.org/hco/8/GRCh38#86224254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19823442-C-A

86224283-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19823413-C-G

http://identifiers.org/hco/8/GRCh38#86224331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19823360-C-A

86224345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19823346-C-T

86224417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19823280-T-C

86225439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19822496-T-C

86225443-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19822492-T-A

86225585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19822320-T-C

http://identifiers.org/hco/8/GRCh38#86226053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19821959-C-A

86226053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19821959-C-T

86226375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19821421-A-G

86226594-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19821209-T-A

86226766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19821091-A-G

86227279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19820551-G-A

86227343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19820489-A-G

86227349-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19820483-T-A

86227349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19820483-T-C

86227470-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19820370-G-T

86229108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19819975-C-T

http://identifiers.org/hco/8/GRCh38#86229217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19819867-C-A

86229278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19819805-G-A

86229279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19819804-A-G

86229418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19819637-G-A

86229505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19819581-T-C

86229511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19819566-T-C

86229542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19819535-T-C

86229542-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19819535-T-G

86229570-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19819514-T-A

86229570-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19819514-T-G

86229571-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19819513-T-G

http://identifiers.org/hco/8/GRCh38#86229681-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19819402-A-C

86229691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 19819392-G-A

86229691-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 19819392-G-C

86229691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 19819392-G-T

86229706-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 19819377-T-A

86229823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 19819260-C-T

http://identifiers.org/hco/8/GRCh38#86230076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19819007-C-A

http://identifiers.org/hco/8/GRCh38#86230380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19818723-C-A

86230380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19818723-C-T

86256076-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19808899-T-A

86258108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19802701-T-C

86258320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19794861-A-G

86258816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19783335-G-T

86258894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19783260-T-C

86259225-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19782940-A-T

86259410-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19782793-C-G

86259416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19782787-A-G

86259615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19782596-T-C

86259899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19782315-C-T

86267886-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19768605-T-A

86267886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19768605-T-C

86271905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19759131-A-G

86271915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19759124-A-G

86271925-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19759114-T-A

86272016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19759022-A-G

86272141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19758943-T-C

86272254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19758816-T-C

86272529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19758665-G-A

86272838-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19758398-T-A

86272867-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19758370-T-A

86273123-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19758214-T-G

86273885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19757471-T-C

86274016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19757342-T-C

86274047-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19757252-G-C

86274170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19757138-A-G

86274617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19756990-G-A

86283879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19753254-T-C

86283994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19753116-G-T

86284022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19753088-A-G

86284022-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19753088-A-T

86284213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19752899-A-G

86284841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19751945-A-G

86284926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19751841-G-A

86284987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19751782-G-A

86285072-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19751696-A-T

http://identifiers.org/hco/8/GRCh38#86285082-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19751686-A-C

86285783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19751118-T-C

http://identifiers.org/hco/8/GRCh38#86285826-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19751073-A-C

86286095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19750761-A-G

86286098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19750758-A-G

86286101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19750755-A-G

86288011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19741008-T-C

86288016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19741003-T-C

86288055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19740951-G-A

86288264-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19740599-A-T

86288337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19740533-T-C

86288499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19740329-G-A

86292509-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19737161-C-G

86299762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19732325-A-G

86299788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19732299-T-C

86299913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19732184-G-A

86300019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19732111-A-G

86300223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19731956-G-A

86300223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19731956-G-T

86300253-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19731926-G-C

86300312-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19731867-T-A

86300393-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19731789-A-T

86300394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19731788-T-C

86300424-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19731760-T-G

86301010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19731275-T-C

86301110-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19731175-A-T

86301492-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19730820-C-G

http://identifiers.org/hco/8/GRCh38#86301560-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19730761-A-C

86301654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19730681-T-C

http://identifiers.org/hco/8/GRCh38#86301753-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19730589-A-C

86302202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19730170-T-C

86302235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19730143-A-G

86304299-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19728027-C-G

86304370-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19727956-A-T

86304614-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19727722-T-A

86304628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19727646-T-C

86305065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19727100-T-C

86305398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19726308-G-T

86305598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19726123-A-G

86305696-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19726026-T-A

86305696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19726026-T-C

86305904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19725828-G-A

86306236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19725506-C-T

86306343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19725408-T-C

86306398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19725367-A-G

86307141-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19725257-G-C

86307216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19725184-T-C

86307318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19725082-A-G

86307441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19724959-A-G

86307477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19724926-T-C

86307543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19724862-C-T

86307553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19724848-A-G

86308288-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19724709-G-C

86308318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19724689-G-A

86308774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19723972-A-G

86308970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19723538-T-C

86319235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19722126-A-G

86319393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19721970-G-T

86320455-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 19719896-T-A

86320475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19719876-C-T

86320509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19719842-A-G

86320509-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19719842-A-T

86320680-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19719690-A-T

86321054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 19719350-A-G

http://identifiers.org/hco/8/GRCh38#86321128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19719265-C-A

86321128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23092
most severe consequence: non coding transcript exon variant
orthologous variants: 19719265-C-T