46743057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: 3 prime UTR variant
orthologous variants: 91451450-G-T

46743354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: 3 prime UTR variant
orthologous variants: 91451190-G-T

http://identifiers.org/hco/11/GRCh38#46743868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#91450709-C-A

46744087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91450503-G-A

46744358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 91450228-G-T

46745061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91449309-A-G

46750282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91446795-G-A

46750495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91446576-G-A

46750740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91446022-G-A

46750740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91446022-G-T

46750991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91445778-T-C

46751298-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91445543-T-A

46751298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91445543-T-C

46751845-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91444273-G-C

46751879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91444239-G-A

46752387-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91443589-C-G

46752420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91443558-A-G

46752588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91443205-G-T

46752614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91443179-A-G

http://identifiers.org/hco/11/GRCh38#46752626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#91443167-C-A

46753511-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91437774-C-G

46753575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91437706-A-G

46753612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91437678-A-G

46754823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91436826-G-A

46754823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91436826-G-T

46754879-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91436776-T-G

http://identifiers.org/hco/11/GRCh38#46755134-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#91436528-A-C

46755593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91436272-G-A

http://identifiers.org/hco/11/GRCh38#46755681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#91436156-C-A

46755724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91436123-T-C

46758772-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91431626-A-T

46758796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91431602-T-C

46759129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91431277-A-G

46759164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91431245-A-G

46759177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91431232-A-G

46759214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91431206-T-C

46759214-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91431206-T-G

46759552-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91430876-T-G

46759568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91430860-T-C

46759568-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91430860-T-G

46759662-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91430774-T-G

46759808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91430639-T-C

46759810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91430637-T-C

46759858-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91430603-C-G

46760230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91430089-T-C

46760246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91430071-T-C

46760471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91429857-T-C

46760499-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91429830-T-A

46760499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91429830-T-C

46760591-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91429742-C-G

46760591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91429742-C-T

46760598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91429735-C-T

46760627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91429706-A-G

46760917-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91429464-T-A

46760973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91429457-G-T

46761216-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91427681-T-A

46761216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91427681-T-C

http://identifiers.org/hco/11/GRCh38#46761454-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#91427370-A-C

46761454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91427370-A-G

46761579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91427227-G-A

http://identifiers.org/hco/11/GRCh38#46761830-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#91427064-A-C

46761830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91427064-A-G

46761866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91427030-G-T

46761907-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91426994-T-G

46761979-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91426921-G-C

46761991-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91426909-G-C

46761991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91426909-G-T

46762532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91426380-G-T

http://identifiers.org/hco/11/GRCh38#46762536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#91426376-C-A

46762536-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91426376-C-G

46762927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91425903-G-A

46762927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91425903-G-T

46763282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91425363-T-C

46763515-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91425141-T-A

46763515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91425141-T-C

46763665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91424989-G-A

46763665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91424989-G-T

46763686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91424968-G-A

46763686-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91424968-G-C

46763686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91424968-G-T

http://identifiers.org/hco/11/GRCh38#46765100-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#91422164-A-C

http://identifiers.org/hco/11/GRCh38#46765138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#91422127-C-A

46765192-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91422073-G-C

46765278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91421987-T-C

46765980-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91421372-T-G

46766097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91421279-A-G

46766217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91421176-T-C

46766271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91420951-T-C

46766551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91420468-T-C

46766601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91420425-A-G

46767440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91419232-T-C

46767505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91419164-A-G

46767661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 91419014-G-A

http://identifiers.org/hco/11/GRCh38#46767689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#91418986-C-A

46767689-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91418986-C-G

46767698-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91418980-T-G

46767806-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91418860-T-A

46767815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91418851-G-A

46767815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91418851-G-T

46767926-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91418761-G-C

46769344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91416937-G-A

46769897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91416760-T-C

46770751-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: 91416294-A-T

http://identifiers.org/hco/11/GRCh38#46771046-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#91415983-A-C

46771046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: 91415983-A-G

http://identifiers.org/hco/11/GRCh38#46771090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#91415937-C-A

46771090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: 91415937-C-T

46776210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: 91411625-A-G

46776693-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: 91411178-G-C

46776901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: 91410984-T-C

46777395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: 91409922-G-A

46777395-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: 91409922-G-C

46777395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: 91409922-G-T

46777401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: 91409916-T-C

46777492-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: missense variant
orthologous variants: 91409826-G-C

46777592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: 91409729-G-T

46778031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: 91408660-G-T

46778043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: 91408647-A-G

46778100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: 91408591-G-T

46778427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: 91408075-A-G

46779528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: 91407077-A-G

http://identifiers.org/hco/11/GRCh38#46780385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#91406460-C-A

46780392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: 91406453-G-A

46780392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: 91406453-G-T

46780617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: 91406319-T-C

http://identifiers.org/hco/11/GRCh38#46780659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#91406277-C-A

46783179-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: 91403492-C-G

46783439-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91403234-G-T

46783442-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91403231-G-C

46783442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91403231-G-T

46784425-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91402937-A-T

46784513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91402851-C-T

http://identifiers.org/hco/11/GRCh38#46784731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#91402635-C-A

46784731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: 91402635-C-T

46787307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: 91401135-A-G

46787358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: 91401093-G-A

46788762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: synonymous variant
orthologous variants: 91400534-T-C

http://identifiers.org/hco/11/GRCh38#46788792-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#91400504-A-C

46788792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: 91400504-A-G

46788804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: 91400493-A-G

46789811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: 91399354-A-G

46789926-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: 91399230-G-T

46789971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: 91399179-A-G

46789992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: 91399158-T-C

46790256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: 91398922-C-T

http://identifiers.org/hco/11/GRCh38#46790308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#91398875-C-A

46790308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: 91398875-C-T

46790569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: synonymous variant
orthologous variants: 91398494-T-C

46790603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: 91398466-T-C

46790619-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: 91398448-T-A

46790619-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: 91398448-T-G

46790645-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: 91398420-T-A

46790645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: 91398420-T-C

46795487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: 91396396-G-A

46795487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: 91396396-G-T

46795493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: 91396390-A-G

http://identifiers.org/hco/11/GRCh38#46795862-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#91395872-A-C

46795862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: 91395872-A-G

46797037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: 91394573-T-C

46797142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: 91394377-C-T

46798029-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91393240-T-A

46798029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91393240-T-C

46800519-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91391914-T-A

46801050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91391528-T-C

46801106-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91391344-T-A

46801106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91391344-T-C

46801170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91391283-G-T

46803080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: 91389912-A-G

46803084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: 91389908-C-T

46808000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: 91389535-C-T

46808073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: synonymous variant
orthologous variants: 91389463-C-T

46808930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, undefined
orthologous variants: 91388542-C-T

46808931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, undefined
orthologous variants: 91388541-G-A

46809294-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: 91388124-T-A

46809477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: missense variant
orthologous variants: 91387941-G-T

46809508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 91387907-G-A

46809508-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 91387907-G-C

46809508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 91387907-G-T

46809523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: 91387883-A-G

46809711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: 91387009-T-C

46809902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: 91386814-A-G

46809902-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: 91386814-A-T

http://identifiers.org/hco/11/GRCh38#46809943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#91386780-C-A

46809943-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: 91386780-C-G

46814878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: 91381407-A-G

http://identifiers.org/hco/11/GRCh38#46815811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#91381153-C-A

46816182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: 91381116-T-C

46817637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: 91380305-T-C

46818026-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: 91379659-G-C

46818280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: 91379339-T-C

46818555-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: 91379074-T-A

http://identifiers.org/hco/11/GRCh38#46818602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#91379042-C-A

46818627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: 91379017-G-A

46818640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: 91379004-G-A

46818640-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: 91379004-G-C

46818640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: 91379004-G-T

46820624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron variant
orthologous variants: 91378172-G-A

http://identifiers.org/hco/11/GRCh38#46820819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#91377978-C-A

46820819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91377978-C-T

46820921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91377913-A-G

46820978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91377853-G-T

46825282-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91370004-A-T

http://identifiers.org/hco/11/GRCh38#46825581-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#91369705-A-C

46826122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91368831-T-C

46826665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91368322-T-C

46826740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91368248-T-C

http://identifiers.org/hco/11/GRCh38#46826773-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#91368215-A-C

46826773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 91368215-A-G

http://identifiers.org/hco/11/GRCh38#46826820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#91368171-C-A

46826820-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91368171-C-G

46826820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91368171-C-T

46826831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91368160-G-A

46826831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91368160-G-T

46826843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 91368153-G-A

46826967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91368029-G-A

46827415-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91367624-G-C

46827416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91367623-G-A

46827847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91367248-G-T

46827925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91367176-G-T

46839252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91361927-G-A

46839252-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91361927-G-C

46839468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91361471-A-G

46840385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91359489-C-T

46845167-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91358236-A-T

46845175-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91358228-T-G

46845199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91358204-G-A

46845388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91358024-G-A

46845388-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91358024-G-C

46846176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91357238-C-T

46846218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28959
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 91357195-A-G