http://identifiers.org/hco/10/GRCh38#101610738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45566768-C-A

101610851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45566872-A-G

101610851-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45566872-A-T

101610930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45566941-G-T

http://identifiers.org/hco/10/GRCh38#101610973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45566983-C-A

101610979-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45566989-T-A

101610979-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45566989-T-G

http://identifiers.org/hco/10/GRCh38#101611168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45567118-C-A

101611351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45567305-G-A

101611402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45567356-C-T

101611520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45567450-T-C

101611520-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45567450-T-G

101611554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45567487-C-T

101611561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45567494-C-T

101611577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45567510-C-T

101611619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45567551-G-A

101611831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45567757-T-C

101611837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45567763-G-A

101611837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45567763-G-T

101612231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45568001-A-G

101612231-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45568001-A-T

101612298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45568059-G-A

101612298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45568059-G-T

101612317-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45568072-T-A

101612317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45568072-T-C

http://identifiers.org/hco/10/GRCh38#101612318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45568073-C-A

101612318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45568073-C-T

http://identifiers.org/hco/10/GRCh38#101612319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45568074-C-A

101612319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45568074-C-T

101612321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45568076-T-C

http://identifiers.org/hco/10/GRCh38#101612330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45568085-C-A

101612330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 45568085-C-T

http://identifiers.org/hco/10/GRCh38#101612426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45568181-C-A

101612426-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45568181-C-G

101612426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45568181-C-T

http://identifiers.org/hco/10/GRCh38#101612520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45568279-C-A

101612520-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45568279-C-G

101612733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45568451-C-T

101613204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45568895-T-C

101613204-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45568895-T-G

101613505-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45569185-C-G

http://identifiers.org/hco/10/GRCh38#101613583-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45569216-A-C

101613685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45569312-C-T

101613733-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45569350-A-T

101613755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45569372-T-C

101614507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45570204-C-T

101614527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45570220-G-A

101614527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45570220-G-T

101614528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45570221-G-A

101614528-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45570221-G-C

101614528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45570221-G-T

101614838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45570468-A-G

101614838-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45570468-A-T

101615038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45570635-C-T

http://identifiers.org/hco/10/GRCh38#101615394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45570989-C-A

101615394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45570989-C-T

101615617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45571229-G-A

101615782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45571464-G-A

101615782-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45571464-G-C

101615782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45571464-G-T

101615842-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45571537-T-A

http://identifiers.org/hco/10/GRCh38#101615845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45571543-C-A

101615918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45571596-C-T

101616136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45571751-A-G

http://identifiers.org/hco/10/GRCh38#101616338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45571927-C-A

101616723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45572193-C-T

101616742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45572211-A-G

101617228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45572585-G-A

101618001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45573764-C-T

101618501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45574150-C-T

101618700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45574340-A-G

http://identifiers.org/hco/10/GRCh38#101618759-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45574395-A-C

101618821-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45574442-G-C

101619173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45574742-T-C

101620063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45575161-C-T

101620683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45575767-G-A

101620711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45575810-C-T

101620879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45575942-A-G

101621041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45576062-T-C

101621045-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45576066-T-A

101623864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45579435-T-C

101624157-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45579579-G-C

101624192-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45579612-T-G

101624214-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45579633-T-G

101624540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45579943-A-G

101624643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45580048-G-T

101624693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45580097-C-T

101624700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45580112-T-C

101624828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45580251-A-G

http://identifiers.org/hco/10/GRCh38#101624939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45580369-C-A

101624961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45580391-G-T

101624966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45580393-A-G

101625016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45580442-A-G

101625175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45580612-A-G

101625203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45580631-G-A

101625203-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45580631-G-C

101625203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45580631-G-T

http://identifiers.org/hco/10/GRCh38#101625208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45580636-C-A

101625208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45580636-C-T

101625209-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45580637-T-A

101625209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45580637-T-C

101625218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45580646-A-G

101625232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45580660-G-A

101625299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45580713-G-A

101625301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45580715-T-C

101625302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45580716-A-G

101625398-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45580896-T-A

101625400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45580898-G-T

101625403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45580901-C-T

101625446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45580950-G-A

101625446-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45580950-G-T

http://identifiers.org/hco/10/GRCh38#101625458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45580961-C-A

101625458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45580961-C-T

http://identifiers.org/hco/10/GRCh38#101625481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45580982-C-A

101625481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45580982-C-T

101625492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45580993-G-A

101625492-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45580993-G-C

101625492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45580993-G-T

101625566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45581049-A-G

101625687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45581162-G-T

101625708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45581183-G-A

101625708-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45581183-G-C

101625708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45581183-G-T

101625749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45581216-C-T

101625815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45581272-G-A

101625815-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45581272-G-C

101625815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45581272-G-T

101625816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45581273-G-A

101625816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45581273-G-T

http://identifiers.org/hco/10/GRCh38#101625888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45581340-C-A

101625888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45581340-C-T

101625943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45581382-A-G

101625943-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45581382-A-T

101625957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45581396-G-T

http://identifiers.org/hco/10/GRCh38#101625966-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45581405-A-C

101625986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45581431-G-A

101626122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45581556-T-C

http://identifiers.org/hco/10/GRCh38#101626131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45581565-C-A

http://identifiers.org/hco/10/GRCh38#101626476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45581870-C-A

101626476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45581870-C-T

101626788-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45581885-A-T

http://identifiers.org/hco/10/GRCh38#101626810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45581908-C-A

101626810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45581908-C-T

101626905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45582023-G-A

101626905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45582023-G-T

101626921-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45582040-T-G

101626923-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45582042-G-C

101626923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45582042-G-T

101626932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45582171-T-C

101626985-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45582222-T-A

101626985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45582222-T-C

101626987-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45582224-T-A

http://identifiers.org/hco/10/GRCh38#101626990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45582227-C-A

101626990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45582227-C-T

101627008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45582245-A-G

http://identifiers.org/hco/10/GRCh38#101627255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45582314-C-A

101627431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45582447-A-G

101627440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45582455-G-A

101627474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45582488-C-T

101628874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45583052-T-C

101628955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45583122-C-T

101629832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45584400-T-C

101629857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45584427-T-C

101629857-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45584427-T-G

101629858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45584428-G-A

101629865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45584435-T-C

101630625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45585184-G-A

101630752-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45585296-T-G

101630887-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45585410-A-T

101631996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45586479-A-G

101632041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45586499-G-A

101632043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45586501-C-T

101638728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45588218-G-A

101639254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45592730-G-A

101639422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45592889-T-C

101639716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45593178-G-A

101639716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45593178-G-T

101639904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45593326-C-T

101640049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45593466-C-T

101640385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45593783-T-C

101643034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45594960-G-A

http://identifiers.org/hco/10/GRCh38#101644381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#45596260-C-A

101644390-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45596269-T-G

101645123-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45598166-C-G

101645843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45598609-G-A

101645853-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45598618-G-C

101645921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45598794-G-A

http://identifiers.org/hco/10/GRCh38#101646531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45599449-C-A

101646531-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45599449-C-G

101646644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45599549-C-T

http://identifiers.org/hco/10/GRCh38#101647109-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45600480-A-C

101647109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45600480-A-G

101647321-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45600673-C-G

101647851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45601107-C-T

101648180-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45601723-T-A

101648218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45601753-A-G

101648486-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45601990-A-T

101648555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45602029-G-A

101648676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45602142-T-C

http://identifiers.org/hco/10/GRCh38#101649224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45602916-C-A

101649231-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45602923-C-G

101649754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45603525-G-A

101649916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45603656-G-A

101649939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45603679-C-T

101649958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45603699-A-G

101650075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45603820-G-A

101650396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45603986-G-A

101650904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45604474-C-T

101651026-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45604577-C-G

101651123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45604648-C-T

101652349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45605862-T-C

101652369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45605881-C-T

101652370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45605882-G-A

101652371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45605883-C-T

101652840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45606853-A-G

101653228-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45607218-A-T

101653546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45607460-A-G

http://identifiers.org/hco/10/GRCh38#101653618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45607530-C-A

http://identifiers.org/hco/10/GRCh38#101658173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45609073-C-A

101658194-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45609094-C-G

101658942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45609500-G-A

101659106-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45609664-T-A

101659174-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45609731-T-A

101659220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45609776-A-G

101659239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45609795-C-T

101659286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45609842-A-G

101659543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45610062-A-G

101660216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45610644-A-G

101660216-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45610644-A-T

101660279-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45610715-T-G

101660298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45610734-C-T

101660347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45610770-G-A

101661082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45612119-A-G

101661102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45612137-G-A

101661208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45612232-G-A

101661412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45612383-A-G

101661513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45612491-C-T

101661677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45612662-C-T

101661825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45612785-G-A

101661842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45612802-C-T

101661881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45612844-C-T

101661891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45612854-T-C

101661891-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45612854-T-G

101661989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45612949-A-G

101662061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45613015-C-T

101662070-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45613024-T-A

http://identifiers.org/hco/10/GRCh38#101662187-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45613131-A-C

101662655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45613580-G-A

101662660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45613585-G-A

101662692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45613619-G-A

101662852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45613761-C-T

101662864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45613773-G-A

101663978-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45614828-T-G

101664060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45615106-G-A

101664060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45615106-G-T

101664317-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45615360-G-C

101664426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45615404-T-C

101665217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45616132-C-T

101665474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45616528-C-T

http://identifiers.org/hco/10/GRCh38#101665517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45616600-C-A

http://identifiers.org/hco/10/GRCh38#101666475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45617494-C-A

101666475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45617494-C-T

101666638-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45617646-G-C

101667549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45619005-G-A

101667556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45619012-G-T

http://identifiers.org/hco/10/GRCh38#101667762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45619185-C-A

101667762-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45619185-C-G

http://identifiers.org/hco/10/GRCh38#101667867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45619285-C-A

101667874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45619292-T-C

101668019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45619437-T-C

101668077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45619498-G-A

101668077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45619498-G-T

101668266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45619668-C-T

101668335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45619736-A-G

101668388-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45619789-G-C

101668411-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45619812-T-A

101669117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45620500-G-A

101669562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45620972-T-C

http://identifiers.org/hco/10/GRCh38#101669567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45620977-C-A

101669567-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45620977-C-G

101671774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45622967-G-A

101671843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45623073-T-C

101671877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45623169-G-A

101672007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45623291-T-C

101672397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45623625-C-T

http://identifiers.org/hco/10/GRCh38#101672701-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45623922-A-C

101672704-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45623925-C-G

101672775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45623998-C-T

101672819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45624039-A-G

http://identifiers.org/hco/10/GRCh38#101672844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45624064-C-A

101672844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45624064-C-T

101672850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45624070-G-T

101672876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45624107-A-G

101672901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45624160-G-A

101672951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45624210-G-A

http://identifiers.org/hco/10/GRCh38#101673076-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45624333-A-C

101673076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45624333-A-G

101673423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45624641-G-A

101673424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45624642-G-T

101673447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45624667-T-C

101673535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45624749-G-A

http://identifiers.org/hco/10/GRCh38#101673543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45624757-C-A

101673543-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45624757-C-G

101673544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45624758-A-G

101674545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45625163-A-G

101674689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45625296-C-T

101674705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45625311-G-A

101674998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45625705-A-G

101675131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45625827-G-A

101675131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45625827-G-T

101675160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45625856-G-A

http://identifiers.org/hco/10/GRCh38#101675745-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45627179-A-C

101676335-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45628859-A-T

101676391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45628915-G-A

101676429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45628953-T-C

101676450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45628974-G-A

101676450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45628974-G-T

101676457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45628981-T-C

http://identifiers.org/hco/10/GRCh38#101676538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45629061-C-A

101676538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45629061-C-T

http://identifiers.org/hco/10/GRCh38#101676540-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45629063-A-C

101676540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45629063-A-G

101676586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45629118-T-C

101676629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45629163-T-C

http://identifiers.org/hco/10/GRCh38#101676644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45629178-C-A

101676644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45629178-C-T

101676836-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45629578-T-A

101676974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45629753-C-T

101677163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45630136-C-T

101677573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45630497-T-C

101677720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45630743-A-G

http://identifiers.org/hco/10/GRCh38#101677928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45630976-C-A

101677986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45631014-G-A

101678037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45631062-A-G

http://identifiers.org/hco/10/GRCh38#101678362-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45631361-A-C

101678735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45631416-C-T

101680216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45633198-G-A

101680642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45633559-C-T

101680810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45633664-T-C

101680957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45633793-C-T

101682132-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45634443-G-C

101682264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45634551-C-T

101682268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45634555-T-C

101682428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45634691-A-G

101682430-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45634693-T-A

101682450-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45634713-T-G

101682760-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45634978-C-G

101682761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45634979-A-G

101682867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45635043-G-T

101682965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45635128-T-C

101682965-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45635128-T-G

101683498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45635623-C-T

101686092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45639778-T-C

101686128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45639808-T-C

101686140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45639820-T-C

101686170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45639844-G-A

101686288-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45639953-G-C

101686892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45640541-G-T

101687269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45640913-C-T

101687350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45640993-C-T

101687485-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45641348-G-C

101687566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45641426-C-T

101687734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45641981-G-T

http://identifiers.org/hco/10/GRCh38#101688250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45642443-C-A

101688637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45642821-A-G

101688888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45643051-G-A

101688888-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45643051-G-T

101688935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45643098-G-T

http://identifiers.org/hco/10/GRCh38#101688971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45643134-C-A

101689017-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45643180-T-G

101689482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45643555-A-G

101689491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45643682-G-T

101689541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45643815-C-T

101689555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45643829-C-T

101689569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45643844-T-C

http://identifiers.org/hco/10/GRCh38#101689712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45644001-C-A

101689727-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45644025-G-C

101689753-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45644049-C-G

http://identifiers.org/hco/10/GRCh38#101689956-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45644251-A-C

101690066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45644357-A-G

101690327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45644577-A-G

http://identifiers.org/hco/10/GRCh38#101690748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45645024-C-A

101690748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45645024-C-T

101690928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45645186-A-G

101690985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45645222-G-A

101691135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45645316-T-C

101691300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45645466-T-C

101691504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45645647-A-G

101691504-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45645647-A-T

101691620-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45645737-C-G

http://identifiers.org/hco/10/GRCh38#101691646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45645774-C-A

101691899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45646218-C-T

http://identifiers.org/hco/10/GRCh38#101692144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45646421-C-A

http://identifiers.org/hco/10/GRCh38#101692231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45646507-C-A

101692346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45646579-A-G

http://identifiers.org/hco/10/GRCh38#101692372-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45646612-A-C

101692917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45646868-G-T

101693036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45646982-G-A

101693145-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45647091-G-C

101693466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45647320-T-C

101693782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45647594-T-C

http://identifiers.org/hco/10/GRCh38#101693832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45647643-C-A

101693930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45647792-G-A

101694017-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45647873-T-A

101694215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45648044-G-A

101694243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45648078-T-C

101694243-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45648078-T-G

101694244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45648079-G-A

101694244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45648079-G-T

http://identifiers.org/hco/10/GRCh38#101694249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#45648084-C-A

101694249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45648084-C-T

101694255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45648090-T-C

101694255-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45648090-T-G

101694270-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45648105-G-C

101694279-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45648114-G-C

101694288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45648123-C-T

101694388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45648222-T-C

101694446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 45648280-A-G

101694446-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45648280-A-T

http://identifiers.org/hco/10/GRCh38#101694655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45648483-C-A

101694655-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45648483-C-G

101694655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45648483-C-T

http://identifiers.org/hco/10/GRCh38#101694784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45648582-C-A

101694784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45648582-C-T

http://identifiers.org/hco/10/GRCh38#101694932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#45648712-C-A

101694932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 45648712-C-T

101694968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 45648748-T-C

101695282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45649042-G-T

http://identifiers.org/hco/10/GRCh38#101695291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#45649051-C-A

101695291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10847
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45649051-C-T