92299088-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 107745668-T-A

92299088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 107745668-T-C

92299139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 107745719-A-G

92299139-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107745719-A-T

92299150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107745730-G-A

92299150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107745730-G-T

http://identifiers.org/hco/1/GRCh38#92299178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107745759-C-A

92299178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107745759-C-T

92299225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107745795-G-A

http://identifiers.org/hco/1/GRCh38#92299276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#107745847-C-A

92299276-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107745847-C-G

92299276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107745847-C-T

http://identifiers.org/hco/1/GRCh38#92299286-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107745857-C-A

92299286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107745857-C-T

http://identifiers.org/hco/1/GRCh38#92299290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#107745861-C-A

92299290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107745861-C-T

92299295-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107745870-T-A

92299295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107745870-T-C

92299295-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107745870-T-G

http://identifiers.org/hco/1/GRCh38#92299336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#107745901-C-A

92299576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107746054-G-A

92299584-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107746062-G-C

92300179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107746369-G-A

92300231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 107746425-T-C

92300290-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107746474-T-A

92300305-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107746489-T-A

http://identifiers.org/hco/1/GRCh38#92300312-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107746496-A-C

92300312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107746496-A-G

92300312-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107746496-A-T

http://identifiers.org/hco/1/GRCh38#92301383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107749504-C-A

92301383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107749504-C-T

http://identifiers.org/hco/1/GRCh38#92301393-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107749514-A-C

92301397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107749521-A-G

92301422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107749539-G-A

92301422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107749539-G-T

92301449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107749570-A-G

92301594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107749715-T-C

92301599-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107749720-T-G

92301630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107749751-A-G

http://identifiers.org/hco/1/GRCh38#92301634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107749755-C-A

92301634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107749755-C-T

92301636-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107749757-T-A

http://identifiers.org/hco/1/GRCh38#92303964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107751379-C-A

92303964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107751379-C-T

http://identifiers.org/hco/1/GRCh38#92304078-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107751493-A-C

http://identifiers.org/hco/1/GRCh38#92304146-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107751543-A-C

92304188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107751588-G-T

http://identifiers.org/hco/1/GRCh38#92304293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107751696-C-A

92304293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 107751696-C-T

92304362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107751765-G-A

92304362-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107751765-G-C

92304469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107751829-A-G

92306996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107754580-G-A

92307250-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 107754833-T-G

92307258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 107754841-G-A

92307358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107754931-G-A

http://identifiers.org/hco/1/GRCh38#92307381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107754954-C-A

92307381-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107754954-C-G

http://identifiers.org/hco/1/GRCh38#92307382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107754955-C-A

92307531-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107755087-T-G

92307532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107755088-G-A

92307627-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107755180-T-A

92307969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107755832-G-A

92308090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107755938-G-A

92308437-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107756235-C-G

92309562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107758058-C-T

92309695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107758321-T-C

92309789-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107758397-T-G

92310932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107759472-T-C

92311092-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107759580-C-G

92311166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107759641-G-A

92311171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107759646-T-C

92315781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107760108-G-T

92315820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107760144-G-A

92315876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107760194-G-T

92316125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107760435-G-A

http://identifiers.org/hco/1/GRCh38#92316624-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107761005-A-C

92316791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107761153-A-G

92316877-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107761201-T-A

92316992-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107761288-A-T

92320123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107765716-A-G

92320159-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107765747-T-G

92320206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107765793-G-A

92320709-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107766087-T-A

92320709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107766087-T-C

92320709-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107766087-T-G

92321065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107766413-T-C

92321214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107766581-G-A

92321478-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107767052-T-A

92321785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107767322-C-T

92321818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107767354-G-A

92323350-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107767629-T-G

92323450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107767693-A-G

92323462-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107767705-A-T

92323470-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107767713-T-A

92323474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107767717-G-A

92323484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 107767727-C-T

92323506-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107767749-A-T

92323510-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107767753-C-G

92323515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107767758-C-T

92323560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107767803-G-A

92323560-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107767803-G-C

92323563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107767806-A-G

92323566-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107767809-A-T

92323572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107767815-G-A

92323661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107767910-A-G

92323663-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107767912-T-A

92323663-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107767912-T-G

92323759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107768002-A-G

92323873-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107768116-A-T

92323895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 107768138-T-C

92323988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 107768231-G-A

92323988-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107768231-G-C

92324080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107768323-A-G

92324330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 107768576-G-T

92324854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron variant
orthologous variants: 107769235-T-C

92325145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron variant
orthologous variants: 107769443-A-G

92325228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron variant
orthologous variants: 107769522-C-T

http://identifiers.org/hco/1/GRCh38#92325656-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107769910-A-C

92325804-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron variant
orthologous variants: 107770053-A-T

92325911-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron variant
orthologous variants: 107770156-T-A

92325911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron variant
orthologous variants: 107770156-T-C

92332323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron variant
orthologous variants: 107770677-G-A

92332699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron variant
orthologous variants: 107771051-G-A

92332752-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron variant
orthologous variants: 107771102-T-G

92332981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron variant
orthologous variants: 107771309-G-T

92333218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron variant
orthologous variants: 107771438-A-G

92333351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 107771547-C-T

92333392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 107771581-A-G

92333486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107771675-T-C

92333491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107771680-A-G

http://identifiers.org/hco/1/GRCh38#92333536-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107771729-A-C

92333536-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107771729-A-T

92333586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107771777-G-A

92333586-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107771777-G-C

92333586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107771777-G-T

http://identifiers.org/hco/1/GRCh38#92333728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107773072-C-A

92333866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107773180-G-A

92333921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107773234-G-A

http://identifiers.org/hco/1/GRCh38#92333998-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107773308-A-C

92334034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107773350-A-G

92336176-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107773620-T-A

http://identifiers.org/hco/1/GRCh38#92336251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107773681-C-A

92336251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107773681-C-T

92336256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107773686-A-G

http://identifiers.org/hco/1/GRCh38#92336395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/5/GRCm39#107773802-C-A

http://identifiers.org/hco/1/GRCh38#92336452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107773860-C-A

92336452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107773860-C-T

92336453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107773861-T-C

92336478-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107773884-T-A

92336556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107773969-T-C

92340054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107776453-T-C

92341512-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107777472-C-G

92345736-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107780847-A-T

92345739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107780850-A-G

92345837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107780920-A-G

http://identifiers.org/hco/1/GRCh38#92345907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107780990-C-A

92345907-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107780990-C-G

http://identifiers.org/hco/1/GRCh38#92346003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107781056-C-A

92346003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107781056-C-T

http://identifiers.org/hco/1/GRCh38#92346006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107781059-C-A

92346006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107781059-C-T

92346917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107781612-T-C

92347549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107782173-T-C

92347577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107782201-T-C

92348323-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107782566-C-G

92348440-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107782663-G-C

92348686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107782883-A-G

92348757-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107782938-T-A

92348880-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107783061-G-C

http://identifiers.org/hco/1/GRCh38#92349166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107783302-C-A

92349166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107783302-C-T

http://identifiers.org/hco/1/GRCh38#92349372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107783469-C-A

92349643-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107783692-C-G

92350015-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107784030-A-T

92350079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107784094-A-G

92351767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107785119-T-C

92352423-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107785623-A-T

http://identifiers.org/hco/1/GRCh38#92352466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107785664-C-A

92353096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107786218-A-G

92353205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107786315-T-C

http://identifiers.org/hco/1/GRCh38#92354046-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107788994-A-C

92354047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107788995-G-T

92354294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107789262-G-A

92354776-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107789715-T-G

92354781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107789720-C-T

92355250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107790055-G-A

92355351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107790117-A-G

92362467-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107791957-G-C

92365714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107796703-G-A

92365843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107796830-G-T

92365980-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107796974-T-A

92366225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107797060-C-T

92366492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107797207-G-A

92366560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107797273-G-A

92366894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107797730-G-A

92367350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107798145-G-A

92367426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107798250-C-T

92367966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107798678-A-G

92369673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107799602-G-A

92370543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

92376626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107801152-C-T

92379476-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107802545-A-T

92379526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107802590-G-T

92380674-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107802978-T-A

92380674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107802978-T-C

http://identifiers.org/hco/1/GRCh38#92380677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107802981-C-A

92380677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107802981-C-T

92380697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107803000-T-C

92380732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107803031-C-T

http://identifiers.org/hco/1/GRCh38#92380911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107803231-C-A

92380911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107803231-C-T

92381238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107803400-G-T

92381352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107803490-T-C

92381396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107803518-A-G

92387062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 107809392-G-A

92387062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 107809392-G-T

92387087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 107809415-G-A

92387087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 107809415-G-T

92387194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 107809448-A-G

92387226-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 107809480-A-T

92387232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 107809483-G-A

92387271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: 3 prime UTR variant
orthologous variants: 107809522-G-A

92387277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: 3 prime UTR variant
orthologous variants: 107809528-G-T

http://identifiers.org/hco/1/GRCh38#92387417-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107809648-A-C

92398615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: 3 prime UTR variant
orthologous variants: 107825929-G-A

92398615-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: 3 prime UTR variant
orthologous variants: 107825929-G-T

92398621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: 3 prime UTR variant
orthologous variants: 107825935-T-C

http://identifiers.org/hco/1/GRCh38#92398751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107826052-C-A

92398751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: 3 prime UTR variant
orthologous variants: 107826052-C-T

92399085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: 3 prime UTR variant
orthologous variants: 107826245-G-A

92399085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: 3 prime UTR variant
orthologous variants: 107826245-G-T

92399188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: 3 prime UTR variant
orthologous variants: 107826348-T-C

92399188-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: 3 prime UTR variant
orthologous variants: 107826348-T-G

92399310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: 3 prime UTR variant
orthologous variants: 107826462-G-A

92399310-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: 3 prime UTR variant
orthologous variants: 107826462-G-T

92399350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: 3 prime UTR variant
orthologous variants: 107826502-G-A

92399376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: 3 prime UTR variant
orthologous variants: 107826528-T-C

92399425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: 3 prime UTR variant
orthologous variants: 107826577-C-T

92399449-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: 3 prime UTR variant
orthologous variants: 107826603-G-T

92399618-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: 3 prime UTR variant
orthologous variants: 107826707-T-G

92399688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: 3 prime UTR variant
orthologous variants: 107826781-A-G

92399781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: 3 prime UTR variant
orthologous variants: 107826838-G-T

92399787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: 3 prime UTR variant
orthologous variants: 107826844-A-G

92399805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: 3 prime UTR variant
orthologous variants: 107826861-G-T

92399820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: 3 prime UTR variant
orthologous variants: 107826876-A-G

92399893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: 3 prime UTR variant
orthologous variants: 107826916-G-A

92399893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: 3 prime UTR variant
orthologous variants: 107826916-G-T

92399905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25791
most severe consequence: 3 prime UTR variant
orthologous variants: 107826928-C-T