236549017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12454970-G-A

236549028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12454959-G-T

236549062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12454954-T-C

236549074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12454942-G-A

236549077-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12454939-C-G

236549170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12454904-C-T

236549584-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12454683-T-G

236549769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12454512-C-T

236550232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 12454150-G-A

http://identifiers.org/hco/1/GRCh38#236550273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12454116-C-A

236550279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 12454110-G-T

http://identifiers.org/hco/1/GRCh38#236550294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12454097-C-A

236550325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: 3 prime UTR variant
orthologous variants: 12454050-G-A

236550325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: 3 prime UTR variant
orthologous variants: 12454050-G-T

236550375-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: 3 prime UTR variant
orthologous variants: 12454023-A-T

236550412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: 3 prime UTR variant
orthologous variants: 12454002-A-G

http://identifiers.org/hco/1/GRCh38#236550517-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12453905-A-C

236550555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: 3 prime UTR variant
orthologous variants: 12453870-A-G

236550722-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: 3 prime UTR variant
orthologous variants: 12453721-A-T

236550724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: 3 prime UTR variant
orthologous variants: 12453719-A-G

236550724-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: 3 prime UTR variant
orthologous variants: 12453719-A-T

236550744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: 3 prime UTR variant
orthologous variants: 12453700-G-A

236550744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: 3 prime UTR variant
orthologous variants: 12453700-G-T

http://identifiers.org/hco/1/GRCh38#236550791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12453669-C-A

236550791-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: 3 prime UTR variant
orthologous variants: 12453669-C-G

236550791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: 3 prime UTR variant
orthologous variants: 12453669-C-T

236550811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: 3 prime UTR variant
orthologous variants: 12453651-A-G

236550811-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: 3 prime UTR variant
orthologous variants: 12453651-A-T

http://identifiers.org/hco/1/GRCh38#236550812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12453650-C-A

236550812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: 3 prime UTR variant
orthologous variants: 12453650-C-T

236551074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 12453405-T-C

236551074-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 12453405-T-G

236551139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 12453371-C-T

236551196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 12453330-G-A

236551196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 12453330-G-T

236551284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 12453237-T-C

236551310-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 12453211-G-T

236551477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 12453110-G-A

236551477-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 12453110-G-C

236551477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 12453110-G-T

236551604-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 12452987-T-A

236551604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 12452987-T-C

236551610-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 12452981-T-A

236551610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 12452981-T-C

236551610-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 12452981-T-G

236551686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 12452934-G-A

236551770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 12452902-G-A

236551770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 12452902-G-T

236551809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 12452874-G-A

236551809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 12452874-G-T

236551945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 12452848-T-C

236551985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 12452835-A-G

236552007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 12452813-A-G

http://identifiers.org/hco/1/GRCh38#236552196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12452619-C-A

236552196-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 12452619-C-G

236552196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 12452619-C-T

236552200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 12452615-T-C

236552299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 12452519-G-A

236553482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12450801-G-A

236553482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12450801-G-T

236553549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12450738-G-T

236553947-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12450412-C-G

http://identifiers.org/hco/1/GRCh38#236554009-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12450364-A-C

236554524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12450148-G-A

236554524-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12450148-G-C

236554524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12450148-G-T

236554529-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12450144-G-T

236554746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: missense variant
orthologous variants: 12449932-G-A

236554779-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12449899-A-T

236554797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12449895-C-T

236554826-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12449872-T-G

236554838-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12449860-T-A

http://identifiers.org/hco/1/GRCh38#236554859-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12449840-A-C

236554886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12449813-G-A

236554886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12449813-G-T

236554901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12449801-T-C

http://identifiers.org/hco/1/GRCh38#236555234-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12449476-A-C

236555234-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12449476-A-T

http://identifiers.org/hco/1/GRCh38#236555235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12449475-C-A

236555235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12449475-C-T

236555328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: missense variant
orthologous variants: 12449389-T-C

236555629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: synonymous variant
orthologous variants: 12449092-C-T

http://identifiers.org/hco/1/GRCh38#236555652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12449069-C-A

236555652-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: missense variant
orthologous variants: 12449069-C-G

236555652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: missense variant
orthologous variants: 12449069-C-T

236555785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12448950-A-G

236555789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12448946-G-A

236555807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 12448928-C-T

236555896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: missense variant
orthologous variants: 12448839-C-T

236555943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 12448792-C-T

236555972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12448764-T-C

http://identifiers.org/hco/1/GRCh38#236556017-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12448726-A-C

236556021-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12448722-T-A

236556035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12448706-A-G

http://identifiers.org/hco/1/GRCh38#236556058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12448684-C-A

236556058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12448684-C-T

236556063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12448679-C-T

236556200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: missense variant
orthologous variants: 12448549-C-T

236556212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: missense variant
orthologous variants: 12448537-T-C

http://identifiers.org/hco/1/GRCh38#236556281-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12448467-A-C

236556281-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12448467-A-T

236556464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12448345-C-T

236556853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12447968-G-T

236556880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12447941-T-C

http://identifiers.org/hco/1/GRCh38#236557056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12447783-C-A

236557056-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12447783-C-G

236557056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12447783-C-T

236557134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12447715-T-C

http://identifiers.org/hco/1/GRCh38#236557176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12447676-C-A

236557176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12447676-C-T

http://identifiers.org/hco/1/GRCh38#236557429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12447424-C-A

236557429-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12447424-C-G

http://identifiers.org/hco/1/GRCh38#236557520-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12447333-A-C

236557547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12447307-A-G

236557643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12447206-T-C

236557747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12447094-C-T

236557749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12447092-A-G

236557873-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12447016-C-G

http://identifiers.org/hco/1/GRCh38#236558118-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12446946-A-C

236558161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12446911-A-G

236558165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12446907-A-G

236558165-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12446907-A-T

236558192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12446880-G-T

236558213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12446864-T-C

236558337-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: missense variant
orthologous variants: 12446751-G-C

236558610-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12446315-T-A

236558610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12446315-T-C

236558623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12446302-A-G

236558630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12446295-C-T

236558679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12446219-G-T

236558736-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12446176-T-A

http://identifiers.org/hco/1/GRCh38#236558752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12446160-C-A

http://identifiers.org/hco/1/GRCh38#236558882-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12446028-A-C

236558882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12446028-A-G

236558882-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12446028-A-T

236558899-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12446011-T-G

236559044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: missense variant
orthologous variants: 12445881-T-C

236559055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: synonymous variant
orthologous variants: 12445870-G-A

http://identifiers.org/hco/1/GRCh38#236559056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12445869-C-A

236559056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: missense variant
orthologous variants: 12445869-C-T

236559128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: missense variant
orthologous variants: 12445797-G-A

236559128-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: missense variant
orthologous variants: 12445797-G-C

236559128-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: missense variant
orthologous variants: 12445797-G-T

http://identifiers.org/hco/1/GRCh38#236559170-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12445751-A-C

236559170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12445751-A-G

236559585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12445291-A-G

236559604-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12445272-T-A

http://identifiers.org/hco/1/GRCh38#236559673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12445194-C-A

236559682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12445184-A-G

236559686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12445180-G-T

236559745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: missense variant
orthologous variants: 12445112-A-G

http://identifiers.org/hco/1/GRCh38#236559878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12444993-C-A

236559878-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12444993-C-G

236559878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12444993-C-T

http://identifiers.org/hco/1/GRCh38#236561299-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12444619-A-C

236561299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12444619-A-G

236561324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12444608-T-C

236561394-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12444562-T-A

236561394-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12444562-T-G

236561454-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12444508-T-A

236561454-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12444508-T-G

236561740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12444206-C-T

236562056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12443594-C-T

236562059-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12443591-T-A

236562059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12443591-T-C

236562119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12443509-G-T

http://identifiers.org/hco/1/GRCh38#236563122-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12442274-A-C

236563122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12442274-A-G

236563145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12442251-T-C

236563145-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12442251-T-G

236563194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12442211-A-G

236564341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12441966-G-A

236564403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12441909-C-T

236564743-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12441574-T-A

236564777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12441541-G-T

236564812-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12441507-T-A

236564812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12441507-T-C

236564839-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12441484-A-T

236564901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12441415-G-A

236566246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12440851-C-T

236566393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12440755-T-C

236566506-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12439860-C-G

http://identifiers.org/hco/1/GRCh38#236566547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12439822-C-A

236566547-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12439822-C-G

236566547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12439822-C-T

http://identifiers.org/hco/1/GRCh38#236566566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12439804-C-A

236566566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12439804-C-T

236566704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: missense variant
orthologous variants: 12439671-A-G

236566811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: synonymous variant
orthologous variants: 12439564-A-G

236566857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: missense variant
orthologous variants: 12439518-A-G

236566935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12439444-T-C

236568158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12439353-C-T

236568207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12439304-T-C

236568270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12439230-T-C

236568271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12439229-G-A

236568986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12438651-G-A

236568986-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12438651-G-C

http://identifiers.org/hco/1/GRCh38#236568987-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12438650-A-C

236571092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12437471-C-T

236571281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12437302-G-A

236571320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12437270-T-C

236571322-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12437268-T-G

236571323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12437267-G-A

http://identifiers.org/hco/1/GRCh38#236571324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12437266-C-A

236571324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12437266-C-T

236571412-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: missense variant
orthologous variants: 12437180-T-A

236571412-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: missense variant
orthologous variants: 12437180-T-G

236571520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12437084-G-A

http://identifiers.org/hco/1/GRCh38#236571555-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12437051-A-C

236571555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12437051-A-G

http://identifiers.org/hco/1/GRCh38#236571557-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12437049-A-C

236571587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: synonymous variant
orthologous variants: 12437019-A-G

236571645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: missense variant
orthologous variants: 12436961-T-C

http://identifiers.org/hco/1/GRCh38#236571961-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12436683-A-C

236572052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12436606-T-C

236572148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12436563-C-T

236572244-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12436472-C-G

236572244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12436472-C-T

http://identifiers.org/hco/1/GRCh38#236572260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12436456-C-A

236572260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12436456-C-T

236572308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12436402-G-T

236572398-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12436313-C-G

236572685-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12436065-G-C

236572861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12435891-T-C

236573882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12434273-A-G

236574002-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12433297-A-T

236574071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12433225-T-C

http://identifiers.org/hco/1/GRCh38#236574222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12433088-C-A

236574519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12432753-T-C

236574611-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12432626-T-G

236574767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 12432475-A-G

236574798-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron_variant, missense_variant
orthologous variants: 12432444-G-C

236574830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron_variant, missense_variant
orthologous variants: 12432412-A-G

http://identifiers.org/hco/1/GRCh38#236575052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12432277-C-A

236575052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12432277-C-T

236575547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12431565-T-C

236575837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12431288-T-C

236575904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12431230-G-A

236575999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12431187-C-T

236576090-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12431102-T-A

236576090-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12431102-T-G

236576112-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12431080-T-A

236576112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12431080-T-C

http://identifiers.org/hco/1/GRCh38#236576119-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12431073-A-C

236576119-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12431073-A-T

236576244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: missense variant
orthologous variants: 12430963-T-C

236576262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: missense variant
orthologous variants: 12430945-A-G

236576440-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12430771-T-A

http://identifiers.org/hco/1/GRCh38#236576459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12430753-C-A

236576459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12430753-C-T

236576481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12430731-A-G

236576485-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12430727-T-A

236581271-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: synonymous variant
orthologous variants: 12429395-A-T

236581526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12429144-T-C

236581672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12428964-C-T

236581793-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12428858-C-G

236581932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12428725-T-C

236582066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12428595-A-G

236582802-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: synonymous variant
orthologous variants: 12428461-C-G

http://identifiers.org/hco/1/GRCh38#236582966-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12428326-A-C

236582966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12428326-A-G

236583004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12428296-G-A

236583004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12428296-G-T

236583138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: missense variant
orthologous variants: 12428162-A-G

236583153-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: missense variant
orthologous variants: 12428147-C-G

http://identifiers.org/hco/1/GRCh38#236583213-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12428087-A-C

236584145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12427891-C-T

236584213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12427830-T-C

236584378-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12427678-T-A

236584378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12427678-T-C

236584734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12427368-G-A

http://identifiers.org/hco/1/GRCh38#236584887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12427252-C-A

236585010-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12427130-T-G

236585037-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: synonymous variant
orthologous variants: 12427103-G-C

236585076-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: missense variant
orthologous variants: 12427064-G-C

236585116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: missense variant
orthologous variants: 12427024-G-T

http://identifiers.org/hco/1/GRCh38#236585276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12426881-C-A

236585295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12426862-T-C

236585319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12426847-G-A

236585319-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12426847-G-C

236585319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12426847-G-T

236585321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12426845-G-A

236585321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12426845-G-T

236585482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12426677-G-A

236585781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12426258-G-T

236585892-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: synonymous variant
orthologous variants: 12426148-T-A

236585960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12426077-T-C

236585988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12426059-C-T

236586046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12425982-T-C

236586078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12425949-G-A

236586078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12425949-G-T

236586448-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: missense variant
orthologous variants: 12425279-C-G

236586448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: missense variant
orthologous variants: 12425279-C-T

236586484-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12425245-G-C

236586484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12425245-G-T

236586543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12425194-G-A

236586543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12425194-G-T

http://identifiers.org/hco/1/GRCh38#236586595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12425137-C-A

236586744-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12425032-A-T

236586815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12424985-A-G

236587147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12424446-T-C

236587159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12424436-T-C

236587251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12424329-G-T

http://identifiers.org/hco/1/GRCh38#236587359-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12424220-A-C

236587392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12424186-G-A

236587392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12424186-G-T

http://identifiers.org/hco/1/GRCh38#236587408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12424170-C-A

236587408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: missense variant
orthologous variants: 12424170-C-T

236587604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12423968-T-C

http://identifiers.org/hco/1/GRCh38#236587871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12423706-C-A

236587871-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12423706-C-G

236587991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: missense variant
orthologous variants: 12423585-T-C

236588085-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12423494-A-T

236588103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12423476-A-G

http://identifiers.org/hco/1/GRCh38#236588139-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12423459-A-C

236588197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12423403-G-A

236588197-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12423403-G-C

236590862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: synonymous variant
orthologous variants: 12422488-G-A

236590862-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: missense variant
orthologous variants: 12422488-G-C

236590862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: synonymous variant
orthologous variants: 12422488-G-T

236590960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 12422390-G-T

236591001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12422357-A-G

236591097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12422279-G-A

236591097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12422279-G-T

236591120-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12422253-T-A

236591157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12422210-T-C

236591314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12422067-T-C

http://identifiers.org/hco/1/GRCh38#236591877-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12421618-A-C

236591877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12421618-A-G

236591877-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12421618-A-T

236591923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12421576-T-C

http://identifiers.org/hco/1/GRCh38#236591956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12421558-C-A

236591956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12421558-C-T

236591963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12421551-T-C

236592115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 12421399-G-A

236592115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 12421399-G-T

http://identifiers.org/hco/1/GRCh38#236592170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12421350-C-A

236592170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12421350-C-T

236592171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12421349-A-G

http://identifiers.org/hco/1/GRCh38#236592182-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12421338-A-C

236592360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12421174-A-G

236592532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: missense variant
orthologous variants: 12421003-A-G

http://identifiers.org/hco/1/GRCh38#236593515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12420522-C-A

236593515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12420522-C-T

236593546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12420492-G-A

236593546-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12420492-G-C

236593658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12420375-A-G

236593709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12420342-A-G

236593873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12420208-G-A

236593873-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12420208-G-C

236593877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12420204-T-C

236593877-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12420204-T-G

236593911-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12420170-T-A

236593911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12420170-T-C

236593914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12420169-A-G

236593914-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12420169-A-T

http://identifiers.org/hco/1/GRCh38#236593926-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12420004-A-C

236593926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12420004-A-G

http://identifiers.org/hco/1/GRCh38#236593937-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12419940-A-C

236593937-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12419940-A-T

236594052-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: missense variant
orthologous variants: 12419829-T-G

236594093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: missense variant
orthologous variants: 12419788-T-C

236594173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12419709-T-C

236595383-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12418302-C-G

236595401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12418283-C-T

http://identifiers.org/hco/1/GRCh38#236595421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12418267-C-A

236595421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12418267-C-T

236595506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12418189-A-G

236595560-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: missense variant
orthologous variants: 12418137-G-C

236595622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: synonymous variant
orthologous variants: 12418075-C-T

http://identifiers.org/hco/1/GRCh38#236595698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12417999-C-A

236595698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12417999-C-T

236595734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12417973-A-G

236595910-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 12417727-A-T

http://identifiers.org/hco/1/GRCh38#236596151-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12417015-A-C

http://identifiers.org/hco/1/GRCh38#236596270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12416890-C-A

236596957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 12416348-C-T

236597675-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12416164-C-G

http://identifiers.org/hco/1/GRCh38#236597808-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12416102-A-C

236597808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12416102-A-G

236597808-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12416102-A-T

236597848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12416063-A-G

236597966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 12415942-G-A

236598090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12415871-T-C

236598129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12415835-A-G

http://identifiers.org/hco/1/GRCh38#236598130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12415834-C-A

236598130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12415834-C-T

236598281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12415704-T-C

236598791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12415072-T-C

236598799-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12415064-T-A

236599447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12413967-T-C

http://identifiers.org/hco/1/GRCh38#236599762-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12413480-A-C

236599887-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12413357-C-G

236600935-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12412516-T-A

236600935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12412516-T-C

http://identifiers.org/hco/1/GRCh38#236600960-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12412490-A-C

236600960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12412490-A-G

236600967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12412483-G-A

236602653-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12411991-G-C

236602654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12411990-G-A

236602756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12411868-C-T

http://identifiers.org/hco/1/GRCh38#236602953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12411660-C-A

http://identifiers.org/hco/1/GRCh38#236603022-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12411607-A-C

236603033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 12411596-T-C

236603166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: missense variant
orthologous variants: 12411511-A-G

http://identifiers.org/hco/1/GRCh38#236603459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12411232-C-A

236603459-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12411232-C-G

http://identifiers.org/hco/1/GRCh38#236603499-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12411202-A-C

236603499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12411202-A-G

236603662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12411045-C-T

236603851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron_variant, undefined
orthologous variants: 12410892-G-A

236603851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron_variant, undefined
orthologous variants: 12410892-G-T

236603886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12410871-A-G

236603886-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12410871-A-T

236603900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron_variant, undefined
orthologous variants: 12410842-A-G

236603900-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron_variant, undefined
orthologous variants: 12410842-A-T

236603941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12410805-A-G

236603949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12410797-C-T

236603965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: missense variant
orthologous variants: 12410781-G-A

236603965-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: missense variant
orthologous variants: 12410781-G-T

http://identifiers.org/hco/1/GRCh38#236604040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12410706-C-A

236604144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12410606-A-G

http://identifiers.org/hco/1/GRCh38#236604174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#12410577-C-A

236604174-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron_variant, undefined
orthologous variants: 12410577-C-G

236604174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron_variant, undefined
orthologous variants: 12410577-C-T

236604251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12410483-A-G

236604305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron variant
orthologous variants: 12410453-G-A

http://identifiers.org/hco/1/GRCh38#236604349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#12410413-C-A

236604349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron_variant, undefined
orthologous variants: 12410413-C-T

http://identifiers.org/hco/1/GRCh38#236604394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#12410380-C-A

236604394-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron_variant, undefined
orthologous variants: 12410380-C-G

236604394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25517
most severe consequence: intron_variant, undefined
orthologous variants: 12410380-C-T