108589538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 48814475-T-C

108589547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 48814466-G-A

108589547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 48814466-G-T

108589612-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: intron_variant, undefined
orthologous variants: 48814403-T-A

108589612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: intron_variant, undefined
orthologous variants: 48814403-T-C

108589612-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: intron_variant, undefined
orthologous variants: 48814403-T-G

108589707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48814281-G-A

108589707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48814281-G-T

http://identifiers.org/hco/3/GRCh38#108589775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#48814215-C-A

108589775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 48814215-C-T

108589790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 48814200-T-C

108589887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 48814097-G-A

108589887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 48814097-G-T

108589890-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 48814094-T-A

108589890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 48814094-T-C

http://identifiers.org/hco/3/GRCh38#108589910-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#48814081-A-C

http://identifiers.org/hco/3/GRCh38#108589911-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#48814080-A-C

108589911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 48814080-A-G

http://identifiers.org/hco/3/GRCh38#108589961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#48814032-C-A

108589961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 48814032-C-T

108589979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 48814007-T-C

108590085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 48813915-G-T

108590175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 48813788-T-C

108590178-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 48813785-G-C

108590329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48813639-T-C

108590333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48813635-C-T

108590389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48813609-T-C

108590389-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48813609-T-G

108590476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48813522-C-T

108590839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48813191-T-C

108597293-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48812462-A-T

108597828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48811952-G-A

108597851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48811931-C-T

108597994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48811808-G-A

108598008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48811789-T-C

108598328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48811481-C-T

108598397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48811411-G-A

108598401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48811407-G-A

108598482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48811345-G-T

108598859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48811030-C-T

108599877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48810303-C-T

108599946-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48810234-G-C

http://identifiers.org/hco/3/GRCh38#108600016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48810162-C-A

108600251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48809597-T-C

108600606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48808869-C-T

108600701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48808774-T-C

108600710-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48808764-T-G

108601064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48808541-A-G

108601448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48808332-T-C

108601592-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48808205-T-G

108601613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48808187-C-T

108602295-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48807944-T-G

http://identifiers.org/hco/3/GRCh38#108602417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48807845-C-A

108602603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48807679-C-T

108602697-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48807597-T-G

108602727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48807564-G-T

108602749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48807541-G-A

http://identifiers.org/hco/3/GRCh38#108603024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48807319-C-A

108603043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48807302-G-T

108603122-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48807226-C-G

108604262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48807116-T-C

108604357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48807009-A-G

108604554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48806831-G-A

108604595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48806789-A-G

108604716-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48806510-T-G

108604806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48806444-C-T

108605194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48805124-A-G

108605286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48805045-G-T

http://identifiers.org/hco/3/GRCh38#108607043-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48803972-A-C

108607350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48803771-A-G

108607473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48803673-A-G

108607900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48802669-A-G

108607940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48802631-A-G

108607992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48802580-T-C

108608128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 48802451-G-A

108610398-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48802130-T-A

108611014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48801578-A-G

108611066-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48801517-A-T

108611154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48801437-T-C

108611333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48801256-A-G

108611356-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48801234-C-G

108611658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48800996-C-T

108616495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48800065-G-T

108616504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48800060-G-T

http://identifiers.org/hco/3/GRCh38#108616506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48800058-C-A

108616652-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 48799912-T-A

http://identifiers.org/hco/3/GRCh38#108616703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48799872-C-A

108616757-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48799835-T-A

108617087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48799695-G-A

108617333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48799457-A-G

108617440-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48799353-T-G

108624337-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48798424-T-A

108624337-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48798424-T-G

http://identifiers.org/hco/3/GRCh38#108624501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48798266-C-A

108624511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 48798256-G-A

108624537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48798228-T-C

108624576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48798189-T-C

108625710-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48796042-A-T

108625733-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48796020-T-G

http://identifiers.org/hco/3/GRCh38#108625824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48795926-C-A

108626005-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48795749-G-C

http://identifiers.org/hco/3/GRCh38#108626074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48795681-C-A

108626074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48795681-C-T

108626479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48795210-G-T

108626630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48795057-A-G

108627676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48794002-T-C

108627741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48793947-C-T

108627816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48793903-C-T

http://identifiers.org/hco/3/GRCh38#108627843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48793871-C-A

108627996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48793730-T-C

108629029-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48792730-T-A

108629308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48792434-A-G

108629308-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48792434-A-T

http://identifiers.org/hco/3/GRCh38#108632750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48781773-C-A

108632750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48781773-C-T

108632846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48781681-G-A

108632846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48781681-G-T

108632904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48781635-A-G

108632980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 48781561-A-G

108633149-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48781349-T-A

108633191-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48781246-T-G

108633193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48781244-A-G

108633243-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48781194-G-C

108634742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48780221-T-C

108634743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48780220-G-T

108634822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48780172-A-G

108634822-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48780172-A-T

108634955-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 48780033-C-G

108634955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 48780033-C-T

108634976-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48780007-T-G

http://identifiers.org/hco/3/GRCh38#108634994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48779989-C-A

108634994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48779989-C-T

108634995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48779988-T-C

108634998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48779981-A-G

http://identifiers.org/hco/3/GRCh38#108635003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48779976-C-A

108635003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48779976-C-T

108635004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48779975-A-G

108635024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48779957-C-T

108635047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48779934-T-C

108635055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48779924-T-C

108635869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48779635-A-G

http://identifiers.org/hco/3/GRCh38#108635903-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48779602-A-C

108635903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48779602-A-G

108636269-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48779243-C-G

108636269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48779243-C-T

108636557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48778927-T-C

108636590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48778897-T-C

108636781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48778727-A-G

108636801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48778705-T-C

108636811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48778695-G-T

108637367-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48778191-T-G

108637388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48778170-T-C

108637556-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 48778006-T-G

http://identifiers.org/hco/3/GRCh38#108637682-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48777869-A-C

108637682-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48777869-A-T

http://identifiers.org/hco/3/GRCh38#108637870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48777696-C-A

108641312-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48775193-A-T

108641402-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48775123-T-G

108641699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48774868-C-T

108642117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48774452-C-T

108642382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48774213-G-A

108642382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48774213-G-T

108642636-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48773988-T-A

108642636-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48773988-T-G

108642659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48773965-G-A

108642659-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48773965-G-C

108642659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48773965-G-T

108642984-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48773664-G-C

108642999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48773650-T-C

108643096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48773521-A-G

108643593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48773063-G-A

108643627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48773029-T-C

http://identifiers.org/hco/3/GRCh38#108643696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48772974-C-A

108643696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48772974-C-T

108643715-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48772961-G-C

108643774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48772903-G-T

108644199-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 48772486-T-G

108644547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 48772138-A-G

http://identifiers.org/hco/3/GRCh38#108644835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48771853-C-A

http://identifiers.org/hco/3/GRCh38#108646544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48770469-C-A

108646544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48770469-C-T

108647825-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48769141-T-A

108647896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48768990-G-A

108647896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48768990-G-T

http://identifiers.org/hco/3/GRCh38#108647930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48768950-C-A

108647930-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48768950-C-G

108647930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48768950-C-T

108648127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48768754-T-C

108648223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48768682-T-C

108648281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48768632-C-T

108648307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48768611-T-C

108648438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48768503-A-G

http://identifiers.org/hco/3/GRCh38#108648484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48768453-C-A

108648484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48768453-C-T

108648552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48768395-T-C

108648597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48768347-T-C

108648890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48768112-A-G

108649639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48767451-G-T

http://identifiers.org/hco/3/GRCh38#108649844-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48767166-A-C

108649844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48767166-A-G

http://identifiers.org/hco/3/GRCh38#108649954-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48767045-A-C

108650088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48766931-T-C

108650088-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48766931-T-G

108650103-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48766916-T-A

108650556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48766455-A-G

108650556-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48766455-A-T

108650763-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48766259-T-A

http://identifiers.org/hco/3/GRCh38#108650872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48766179-C-A

108650872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48766179-C-T

108651094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48766031-G-A

108651094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48766031-G-T

108651252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48765891-A-G

108651290-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48765861-T-A

108654410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48765011-A-G

108654469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48764959-A-G

108655432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48764148-A-G

108661833-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48763954-T-A

108661967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 48763823-T-C

http://identifiers.org/hco/3/GRCh38#108662184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48762510-C-A

http://identifiers.org/hco/3/GRCh38#108662335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#48762368-C-A

108662335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 48762368-C-T

108669541-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48762194-T-A

108669544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48762188-A-G

108669614-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48762128-G-C

108669718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 48762044-A-G

108669762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48762003-C-T

108669776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48761989-G-A

http://identifiers.org/hco/3/GRCh38#108669785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48761980-C-A

108669785-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48761980-C-G

108669785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48761980-C-T

108669819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48761957-G-A

108669819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48761957-G-T

108669871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48761913-G-T

108669875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48761909-A-G

108669875-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48761909-A-T

108669878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48761906-A-G

108670198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48761606-G-T

108670283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48761512-G-T

108670409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48761394-G-A

http://identifiers.org/hco/3/GRCh38#108670692-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48761291-A-C

108671863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48760156-A-G

108672207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48759261-G-T

108672469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48758981-A-G

108672542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48758909-A-G

108672797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48758670-G-T

108672978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48758511-A-G

108673274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48758201-A-G

108673276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48758199-C-T

108673295-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48758180-G-C

108673335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48758152-G-A

108673506-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48757990-T-G

108673755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48757743-T-C

108674023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48757481-T-C

108674792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48756889-C-T

108674959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48756782-A-G

108675568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48756167-T-C

http://identifiers.org/hco/3/GRCh38#108675647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48756094-C-A

108675647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48756094-C-T

108675737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48755995-G-A

108675737-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48755995-G-C

108675737-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48755995-G-T

108675775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48755958-T-C

108675900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48755835-A-G

http://identifiers.org/hco/3/GRCh38#108676784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48755157-C-A

108677079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48754824-A-G

108677403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48754343-A-G

108677403-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48754343-A-T

108677485-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant, synonymous_variant
orthologous variants: 48754268-T-G

108678511-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48753771-G-C

http://identifiers.org/hco/3/GRCh38#108682994-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48752886-A-C

http://identifiers.org/hco/3/GRCh38#108683195-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48752612-A-C

108683285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48752513-T-C

108683560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48752261-A-G

108683663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48752187-G-A

108683786-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48752057-C-G

http://identifiers.org/hco/3/GRCh38#108683800-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48752040-A-C

108684100-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48751762-T-A

108684100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48751762-T-C

108684162-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48751707-T-A

108684162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48751707-T-C

108684348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 48751521-G-A

108684348-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 48751521-G-C

108684358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48751511-T-C

108684544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48751351-A-G

108684703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48751228-A-G

http://identifiers.org/hco/3/GRCh38#108684739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48751212-C-A

108684763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48751195-G-T

108684778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48751184-G-T

108684790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48751171-A-G

108684849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48751113-C-T

108684973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48750976-G-A

108686415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48750145-T-C

108686698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48749879-A-G

108686879-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48749709-C-G

108686899-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48749686-A-T

108687045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48749542-T-C

108688113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48748640-A-G

108688227-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48748532-G-C

108688227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48748532-G-T

108688469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48748323-T-C

108689050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48747771-G-A

108689050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48747771-G-T

http://identifiers.org/hco/3/GRCh38#108689074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48747747-C-A

108689319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48747526-A-G

108690466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48746767-G-A

108691062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48746189-G-A

108693497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 48745755-T-C

108693506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 48745746-C-T

108694012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 48745254-G-A

108694260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30938
most severe consequence: 3 prime UTR variant
orthologous variants: 48745007-A-G