87980278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: 3 prime UTR variant
orthologous variants: 100454020-T-C

87980452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron variant
orthologous variants: 100453835-G-A

87980452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron variant
orthologous variants: 100453835-G-T

http://identifiers.org/hco/12/GRCh38#87980501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#100453779-C-A

87980501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron variant
orthologous variants: 100453779-C-T

http://identifiers.org/hco/12/GRCh38#87980728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#100453542-C-A

87980803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron variant
orthologous variants: 100453456-A-G

http://identifiers.org/hco/12/GRCh38#87981076-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#100452879-A-C

http://identifiers.org/hco/12/GRCh38#87981322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#100452565-C-A

87981329-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron variant
orthologous variants: 100452558-T-G

87981926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron variant
orthologous variants: 100451979-C-T

87981967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron variant
orthologous variants: 100451939-A-G

87982335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron variant
orthologous variants: 100451716-G-A

87982627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron variant
orthologous variants: 100451484-C-T

87982628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron variant
orthologous variants: 100451483-G-A

87982797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron variant
orthologous variants: 100451373-G-A

87983079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron variant
orthologous variants: 100451174-T-C

87983079-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron variant
orthologous variants: 100451174-T-G

http://identifiers.org/hco/12/GRCh38#87983120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#100451133-C-A

87983168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: missense variant
orthologous variants: 100451085-T-C

87983381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100450867-T-C

87983381-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100450867-T-G

87984540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100450063-G-A

87984543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100450060-G-T

87984571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100450032-G-A

87984586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100450017-T-C

87984624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100449960-G-T

87984682-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100449889-C-G

http://identifiers.org/hco/12/GRCh38#87984801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#100449746-C-A

87984801-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100449746-C-G

87984956-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100449612-C-G

87985204-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100449433-G-C

87985204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100449433-G-T

http://identifiers.org/hco/12/GRCh38#87985448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#100449217-C-A

87985564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100449101-G-A

87985564-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100449101-G-C

87985564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100449101-G-T

87985599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100449066-T-C

87985600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100449065-G-T

87985651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100449015-A-G

87985657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100449009-G-A

87985678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100448988-A-G

87985678-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100448988-A-T

87985695-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100448967-A-T

http://identifiers.org/hco/12/GRCh38#87985722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#100448932-C-A

87985722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100448932-C-T

87985746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100448908-A-G

87985798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100448862-A-G

87985799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100448861-T-C

87985909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 100448754-G-A

87985962-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 100448701-T-G

87985973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 100448690-T-C

87986091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100448573-G-A

87986091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100448573-G-T

87986107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100448557-A-G

http://identifiers.org/hco/12/GRCh38#87986122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#100448543-C-A

87986122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100448543-C-T

87986175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100448488-G-A

87986175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100448488-G-T

87986421-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 100448284-G-C

87986455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100448249-G-T

87986458-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100448246-T-G

87986478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100448225-A-G

http://identifiers.org/hco/12/GRCh38#87986540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#100448174-C-A

87986635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100448077-T-C

http://identifiers.org/hco/12/GRCh38#87986970-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#100447738-A-C

87986970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100447738-A-G

87987045-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100447664-T-G

87987254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100447497-C-T

87987350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100447417-T-C

87987370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100447397-C-T

87987856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 100446569-A-G

87987874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 100446551-T-C

87987923-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 100446502-T-G

87987966-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 100446459-T-A

87987989-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100446437-T-A

87988022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100446414-T-C

87988085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100446391-T-C

87988092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100446385-G-A

87988092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100446385-G-T

87988312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100446163-T-C

87988312-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100446163-T-G

87988479-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100445998-T-A

87988543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100445946-T-C

87988820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100445546-G-A

87989116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100445266-C-T

http://identifiers.org/hco/12/GRCh38#87989196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#100445185-C-A

87989196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100445185-C-T

87989218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100445162-G-A

87989218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100445162-G-T

http://identifiers.org/hco/12/GRCh38#87989338-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#100445043-A-C

87989341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 100445040-A-G

87989341-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 100445040-A-T

87989389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100444992-T-C

87989389-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100444992-T-G

87989396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100444985-G-A

87989418-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100444963-A-T

87989460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100444920-T-C

87989460-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100444920-T-G

87989684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100444876-A-G

87992161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100443470-A-G

87992165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100443466-C-T

87992424-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100443311-T-G

87992438-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100443297-C-G

87992598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100443139-C-T

87992607-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100443128-A-T

87992688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100442987-T-C

87992763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100442901-T-C

87993236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100442436-A-G

87993342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100442321-G-A

87993342-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100442321-G-C

87993342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100442321-G-T

87993494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100442251-C-T

87993658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100442152-T-C

87993843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100441973-C-T

87994340-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100441813-C-G

87994441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100441737-G-A

87994493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100441685-C-T

87994504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100441674-A-G

87994504-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100441674-A-T

http://identifiers.org/hco/12/GRCh38#87994517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#100441661-C-A

87994517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100441661-C-T

87994534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100441652-A-G

87994534-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100441652-A-T

http://identifiers.org/hco/12/GRCh38#87994575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#100441618-C-A

87994592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100441615-T-C

87994725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 100441493-G-A

87994725-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 100441493-G-C

http://identifiers.org/hco/12/GRCh38#87994813-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#100441425-A-C

87994813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100441425-A-G

87994838-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100441400-T-A

87995043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100441211-G-A

87995107-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100441162-G-C

87995130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100441149-C-T

87995229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100441036-A-G

87995230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100441035-T-C

87995248-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100441019-T-G

87995797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100440122-C-T

http://identifiers.org/hco/12/GRCh38#87996058-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#100439794-A-C

87996251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100439603-T-C

http://identifiers.org/hco/12/GRCh38#87996496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#100439352-C-A

87996496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100439352-C-T

87996531-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100439318-T-A

87996607-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 100439242-T-G

87996650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 100439199-T-C

87996679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100439168-C-T

http://identifiers.org/hco/12/GRCh38#87996695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#100439152-C-A

87996695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100439152-C-T

87996717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100439130-G-A

87996717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100439130-G-T

87996744-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100439103-A-T

http://identifiers.org/hco/12/GRCh38#87996765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#100439075-C-A

87996765-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100439075-C-G

87996878-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100438964-C-G

87996878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100438964-C-T

87997143-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100438741-T-A

87997143-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100438741-T-G

87997813-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100438031-T-G

http://identifiers.org/hco/12/GRCh38#87997983-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#100437932-A-C

87998002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100437914-G-A

87998002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100437914-G-T

http://identifiers.org/hco/12/GRCh38#87998251-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#100437668-A-C

88011415-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100437007-G-C

http://identifiers.org/hco/12/GRCh38#88026602-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#100430901-A-C

88026645-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100430861-G-C

88026645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100430861-G-T

88026648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100430858-G-T

88026678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100430835-A-G

88026679-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100430834-A-T

88026685-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100430828-C-G

88026685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100430828-C-T

88026716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100430808-G-T

88026800-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100430649-T-A

http://identifiers.org/hco/12/GRCh38#88026825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#100430631-C-A

http://identifiers.org/hco/12/GRCh38#88026835-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#100430621-A-C

88026849-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100430609-G-C

88026885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100430576-A-G

88026888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100430573-A-G

http://identifiers.org/hco/12/GRCh38#88027123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#100430349-C-A

88027165-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100430311-G-C

88027165-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100430311-G-T

88027353-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100430147-G-C

88027403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100430104-C-T

88027621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100429904-G-T

http://identifiers.org/hco/12/GRCh38#88027624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#100429901-C-A

88027624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100429901-C-T

88027627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100429898-T-C

88027633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100429892-T-C

88027664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100429865-T-C

http://identifiers.org/hco/12/GRCh38#88027731-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#100429790-A-C

http://identifiers.org/hco/12/GRCh38#88027738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#100429783-C-A

88027738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100429783-C-T

88027890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100429647-T-C

88027923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100429622-T-C

88027961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100429583-A-G

88027961-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100429583-A-T

88027978-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100429566-T-G

88028234-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100429265-G-C

88028413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100429080-G-T

88029186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100428443-A-G

88029186-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100428443-A-T

http://identifiers.org/hco/12/GRCh38#88029238-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#100428391-A-C

88029495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100428156-G-T

88029507-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100428144-G-C

88029507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100428144-G-T

88029625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100428039-T-C

88029723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100427951-C-T

http://identifiers.org/hco/12/GRCh38#88030023-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#100427613-A-C

http://identifiers.org/hco/12/GRCh38#88030056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#100427584-C-A

88030057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100427583-A-G

88032630-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100427323-A-T

88033708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26665
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100426702-C-T