76444925-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: non coding transcript exon variant
orthologous variants: 98305882-G-C

76445386-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98305421-T-G

76445662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98305155-C-T

76446103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98304744-C-T

76446249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98304627-G-A

76446847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98304099-T-C

http://identifiers.org/hco/11/GRCh38#76447056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98303870-C-A

76447095-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98303822-T-A

76447095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98303822-T-C

76447137-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98303770-A-T

http://identifiers.org/hco/11/GRCh38#76447184-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98303717-A-C

76447423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98303524-G-A

76447716-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98303002-A-T

76448100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98302734-C-T

76448377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98302513-C-T

76448902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98300657-T-C

76449064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98300505-A-G

76449296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98300159-A-G

76449798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98299181-A-G

http://identifiers.org/hco/11/GRCh38#76451996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98296968-C-A

76451996-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98296968-C-G

76451996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98296968-C-T

76452414-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98296474-T-A

76452802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98296181-T-C

http://identifiers.org/hco/11/GRCh38#76453500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98295540-C-A

76453500-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 98295540-C-G

76453510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 98295530-G-T

76453557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 98295482-G-A

76453557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 98295482-G-T

76453635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 98295404-A-G

76453671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 98295394-T-C

76454121-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98294972-T-G

76454353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98294747-T-C

76454572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98294551-G-A

http://identifiers.org/hco/11/GRCh38#76454698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98294464-C-A

76454698-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98294464-C-G

76455673-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 98293521-A-T

76455687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 98293497-T-C

76455701-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 98293477-A-T

76456371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98292907-C-T

76456454-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98292826-C-G

76456681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98292600-G-A

76456894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98292200-C-T

76457220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98291848-G-A

76457642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98291376-C-T

76457801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98291221-G-A

76457865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98291159-T-C

76458622-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98290330-T-A

76458622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98290330-T-C

76458622-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98290330-T-G

76458716-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98290260-A-T

76458840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98290160-G-A

http://identifiers.org/hco/11/GRCh38#76459145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#98289861-C-A

76459145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 98289861-C-T

76459310-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98289681-G-T

76459406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98289594-T-C

76459446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98289560-G-A

76459446-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98289560-G-T

76459457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98289549-G-A

76459457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98289549-G-T

76459463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98289542-G-A

76459463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98289542-G-T

76459596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98289405-A-G

http://identifiers.org/hco/11/GRCh38#76459854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98289169-C-A

76459854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98289169-C-T

76460281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98288742-G-A

http://identifiers.org/hco/11/GRCh38#76463673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98286873-C-A

76463689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98286857-A-G

76463697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98286849-A-G

76463697-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98286849-A-T

76463730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98286812-A-G

76464046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 98286500-C-T

76464138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98286413-G-A

76464181-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98286377-T-A

http://identifiers.org/hco/11/GRCh38#76464198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98286360-C-A

76464223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98286340-A-G

76464223-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98286340-A-T

76465473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98285281-A-G

76467068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98284470-A-G

76467241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98284177-G-A

76467476-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98283950-A-T

76468511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98283169-T-C

76469006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98282672-C-T

76469414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98282300-A-G

76469555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98282165-T-C

76469555-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98282165-T-G

http://identifiers.org/hco/11/GRCh38#76469710-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98282022-A-C

76469837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98281881-C-T

http://identifiers.org/hco/11/GRCh38#76469902-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98281821-A-C

76469953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98281767-A-G

http://identifiers.org/hco/11/GRCh38#76469978-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98281748-A-C

76470857-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98280992-T-G

76470980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98280882-C-T

76471684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98280414-G-A

76471908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98280237-C-T

76471950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98280213-A-G

76471959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98280204-T-C

76472511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98279667-A-G

76477759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98278775-G-A

76478132-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98278497-C-G

76478360-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98278414-T-G

76478367-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98278407-T-A

76478367-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98278407-T-G

76478909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98278072-T-C

76488015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98277282-T-C

http://identifiers.org/hco/11/GRCh38#76488749-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98276570-A-C

76488749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98276570-A-G

76488975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98276390-G-A

http://identifiers.org/hco/11/GRCh38#76489087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98276288-C-A

76496372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 98275768-A-G

76496427-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 98275713-C-G

76496434-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 98275706-G-C

76496610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98275544-A-G

76496610-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98275544-A-T

76496671-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98275487-A-T

76496746-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98275416-T-A

76496764-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98275398-C-G

76496854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98275300-T-C

76497008-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98275147-G-C

76511739-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron variant
orthologous variants: 98272476-C-G

76511853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron variant
orthologous variants: 98272367-G-T

76511891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron variant
orthologous variants: 98272336-C-T

76512221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron variant
orthologous variants: 98272057-T-C

76513161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron variant
orthologous variants: 98270944-A-G

76513303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron variant
orthologous variants: 98270821-G-A

76513303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron variant
orthologous variants: 98270821-G-T

76513366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron variant
orthologous variants: 98270765-T-C

76513758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron variant
orthologous variants: 98270204-A-G

http://identifiers.org/hco/11/GRCh38#76515094-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98269631-A-C

76515094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron variant
orthologous variants: 98269631-A-G

76515094-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron variant
orthologous variants: 98269631-A-T

76515125-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron variant
orthologous variants: 98269606-T-G

76515485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron variant
orthologous variants: 98269270-T-C

76515710-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron variant
orthologous variants: 98269069-C-G

76515994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron variant
orthologous variants: 98268822-A-G

76516363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 98268455-A-G

76516392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 98268426-A-G

76516446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 98268370-G-A

76516446-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 98268370-G-T

76516484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 98268332-A-G

76516522-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 98268294-A-T

76516744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 98268125-C-T

http://identifiers.org/hco/11/GRCh38#76516958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98267916-C-A

76517194-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron variant
orthologous variants: 98267681-T-G

76517920-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron variant
orthologous variants: 98267061-T-A

76517949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron variant
orthologous variants: 98267033-T-C

76518025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron variant
orthologous variants: 98266968-G-A

http://identifiers.org/hco/11/GRCh38#76523045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98264929-C-A

76523056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron variant
orthologous variants: 98264918-G-A

76523056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron variant
orthologous variants: 98264918-G-T

76523302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron variant
orthologous variants: 98264670-G-A

76523302-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron variant
orthologous variants: 98264670-G-C

76523307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron variant
orthologous variants: 98264665-A-G

76523672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron variant
orthologous variants: 98264348-G-A

76523686-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron variant
orthologous variants: 98264334-A-T

76525081-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron variant
orthologous variants: 98263731-T-A

76525658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron variant
orthologous variants: 98263068-A-G

76525866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron variant
orthologous variants: 98262943-A-G

76526230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron variant
orthologous variants: 98262603-C-T

76526318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron variant
orthologous variants: 98262519-G-A

76526318-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron variant
orthologous variants: 98262519-G-C

76526318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron variant
orthologous variants: 98262519-G-T

76526417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron variant
orthologous variants: 98262404-T-C

76526487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 98262337-C-T

76526568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 98262256-C-T

76526687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98262114-T-C

76527066-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98261513-G-C

76527455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98261172-G-A

76527581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98261046-G-A

76528493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98259846-T-C

http://identifiers.org/hco/11/GRCh38#76528504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98259836-C-A

76528504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98259836-C-T

76528507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98259833-A-G

http://identifiers.org/hco/11/GRCh38#76528518-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98259822-A-C

76528729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98259629-A-G

76528759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98259606-T-C

76529221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98259104-G-A

76529280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98258985-A-G

76529480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98258560-T-C

76529480-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98258560-T-G

76529921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98258039-T-C

76531964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98256541-C-T

76532351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98256312-G-T

76532884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98255598-A-G

76532890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98255592-A-G

http://identifiers.org/hco/11/GRCh38#76533107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98255415-C-A

76533356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98255215-A-G

76533356-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98255215-A-T

76533475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98255086-A-G

76533532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98254991-T-C

76533863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98254634-C-T

76533867-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98254630-G-C

76534928-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98252910-T-G

76535458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98252339-A-G

76535510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98252287-C-T

76536079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98251768-A-G

76536143-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98251723-T-A

http://identifiers.org/hco/11/GRCh38#76536190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98251712-C-A

76536190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98251712-C-T

76536369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98251553-A-G

76536448-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98251469-A-T

76537063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98250931-T-C

76537539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98250266-G-A

76537674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98250151-G-A

http://identifiers.org/hco/11/GRCh38#76537994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98249836-C-A

76538010-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98249820-G-T

76539463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98249136-G-A

76539463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98249136-G-T

76539529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98249069-G-A

76539538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98249061-A-G

http://identifiers.org/hco/11/GRCh38#76539577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98249021-C-A

76539676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98248921-G-A

76539676-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98248921-G-C

76539911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98248704-T-C

76539911-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98248704-T-G

76540098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98248501-G-A

76540307-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98247850-T-A

76540521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98247628-C-T

http://identifiers.org/hco/11/GRCh38#76540717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98247468-C-A

76541973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98246628-T-C

76542135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98246477-C-T

76542372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98246233-T-C

76542378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98246227-T-C

76542384-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98246224-T-G

76542404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98246204-T-C

76543394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98245322-G-A

76543407-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98245309-T-G

76543438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98245278-G-A

http://identifiers.org/hco/11/GRCh38#76543456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98245260-C-A

76543937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98244823-G-A

76544029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98244744-G-A

76544127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98244647-G-T

http://identifiers.org/hco/11/GRCh38#76544234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98244542-C-A

76544538-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 98244238-C-G

76544538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 98244238-C-T

http://identifiers.org/hco/11/GRCh38#76544566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98244210-C-A

76544566-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 98244210-C-G

76544566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 98244210-C-T

76544589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 98244187-C-T

76544621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 98244155-C-T

76544646-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 98244130-C-G

76544676-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 98244100-G-C

76544891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 98243866-G-A

76544891-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 98243866-G-C

76544891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 98243866-G-T

76544902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 98243855-G-A

76544902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 98243855-G-T

76545291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron variant
orthologous variants: 98243531-C-T

76545362-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron variant
orthologous variants: 98243458-A-T

http://identifiers.org/hco/11/GRCh38#76545672-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98243139-A-C

76545672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron variant
orthologous variants: 98243139-A-G

76545885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, missense_variant
orthologous variants: 98242927-G-A

76546179-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, missense_variant
orthologous variants: 98242654-C-G

76546364-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron variant
orthologous variants: 98242475-T-A

http://identifiers.org/hco/11/GRCh38#76547006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98241871-C-A

76547018-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron variant
orthologous variants: 98241859-T-A

http://identifiers.org/hco/11/GRCh38#76547023-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98241856-A-C

76547107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 98241771-G-A

76547126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron variant
orthologous variants: 98241745-G-A

76547126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron variant
orthologous variants: 98241745-G-T

76547296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron variant
orthologous variants: 98241551-C-T

76547331-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron variant
orthologous variants: 98241516-A-T

76547599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron variant
orthologous variants: 98241282-C-T

76549694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron variant
orthologous variants: 98240312-A-G

76549715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron variant
orthologous variants: 98240293-A-G

http://identifiers.org/hco/11/GRCh38#76549865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98240179-C-A

76549865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron variant
orthologous variants: 98240179-C-T

http://identifiers.org/hco/11/GRCh38#76549880-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98240174-C-A

76549880-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron variant
orthologous variants: 98240174-C-G

76549880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron variant
orthologous variants: 98240174-C-T

http://identifiers.org/hco/11/GRCh38#76549886-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98240168-A-C

76549886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron variant
orthologous variants: 98240168-A-G

76549886-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: intron variant
orthologous variants: 98240168-A-T

http://identifiers.org/hco/11/GRCh38#76550396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98239649-C-A

76550396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: 3 prime UTR variant
orthologous variants: 98239649-C-T

http://identifiers.org/hco/11/GRCh38#76550707-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98239343-A-C

76550838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: 3 prime UTR variant
orthologous variants: 98239238-G-T

76551412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: 3 prime UTR variant
orthologous variants: 98238682-C-T

76551469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: 3 prime UTR variant
orthologous variants: 98238627-G-A

76552035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: 3 prime UTR variant
orthologous variants: 98238041-A-G

76552192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: 3 prime UTR variant
orthologous variants: 98237879-A-G

76552192-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: 3 prime UTR variant
orthologous variants: 98237879-A-T

76552290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: 3 prime UTR variant
orthologous variants: 98237781-T-C

76552799-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: 3 prime UTR variant
orthologous variants: 98236056-A-T

76552816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: 3 prime UTR variant
orthologous variants: 98236039-C-T

76552840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: 3 prime UTR variant
orthologous variants: 98236018-C-T

http://identifiers.org/hco/11/GRCh38#76552939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18071
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98235928-C-A