44379687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3 prime UTR variant
orthologous variants: 6053072-G-T

44379811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3 prime UTR variant
orthologous variants: 6053190-G-T

44379857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3 prime UTR variant
orthologous variants: 6053255-G-A

44379857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3 prime UTR variant
orthologous variants: 6053255-G-T

44379858-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3 prime UTR variant
orthologous variants: 6053256-G-C

44379858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3 prime UTR variant
orthologous variants: 6053256-G-T

44379963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3 prime UTR variant
orthologous variants: 6053362-G-A

http://identifiers.org/hco/7/GRCh38#44380058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6053451-C-A

http://identifiers.org/hco/7/GRCh38#44380066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6053459-C-A

44380119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3 prime UTR variant
orthologous variants: 6053490-G-A

44380140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3 prime UTR variant
orthologous variants: 6053511-A-G

44381087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3 prime UTR variant
orthologous variants: 6053630-A-G

44381087-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3 prime UTR variant
orthologous variants: 6053630-A-T

44381088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3 prime UTR variant
orthologous variants: 6053631-G-A

44381088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3 prime UTR variant
orthologous variants: 6053631-G-T

44382393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3 prime UTR variant
orthologous variants: 6054575-T-C

44382426-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3 prime UTR variant
orthologous variants: 6054606-C-G

44382535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3 prime UTR variant
orthologous variants: 6054683-A-G

44382689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3 prime UTR variant
orthologous variants: 6054849-C-T

http://identifiers.org/hco/7/GRCh38#44382738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6054891-C-A

44382738-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3 prime UTR variant
orthologous variants: 6054891-C-G

44382738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3 prime UTR variant
orthologous variants: 6054891-C-T

http://identifiers.org/hco/7/GRCh38#44383114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6055258-C-A

http://identifiers.org/hco/7/GRCh38#44383224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6055342-C-A

44383224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3 prime UTR variant
orthologous variants: 6055342-C-T

44383230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3 prime UTR variant
orthologous variants: 6055348-G-T

44383246-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3 prime UTR variant
orthologous variants: 6055359-T-A

44383246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3 prime UTR variant
orthologous variants: 6055359-T-C

44383285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3 prime UTR variant
orthologous variants: 6055448-A-G

http://identifiers.org/hco/7/GRCh38#44383289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6055452-C-A

http://identifiers.org/hco/7/GRCh38#44383302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6055469-C-A

44383302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3 prime UTR variant
orthologous variants: 6055469-C-T

44383304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3 prime UTR variant
orthologous variants: 6055471-C-T

http://identifiers.org/hco/7/GRCh38#44383401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6055823-C-A

44383401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3 prime UTR variant
orthologous variants: 6055823-C-T

44383446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3 prime UTR variant
orthologous variants: 6055848-C-T

http://identifiers.org/hco/7/GRCh38#44383503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6055902-C-A

44383516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3 prime UTR variant
orthologous variants: 6055914-G-A

44383541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3 prime UTR variant
orthologous variants: 6055939-T-C

44383599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6055993-T-C

44383615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6056009-A-G

44383668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6056061-G-A

44383668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6056061-G-T

44383798-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6056186-T-A

44383798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6056186-T-C

44383950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6056339-G-A

44384017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6056404-G-T

44384131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6056514-T-C

http://identifiers.org/hco/7/GRCh38#44384136-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6056518-C-A

44384388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6056742-A-G

http://identifiers.org/hco/7/GRCh38#44384502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6056853-C-A

44384637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6057013-T-C

44384705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6057084-G-A

44384705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6057084-G-T

http://identifiers.org/hco/7/GRCh38#44384715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6057101-C-A

44384715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6057101-C-T

44384746-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6057137-G-C

44384746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6057137-G-T

44384781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6057167-G-A

44384816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6057187-T-C

44384817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6057188-G-T

44385105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6057377-A-G

44385242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6057500-G-A

44385242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6057500-G-T

http://identifiers.org/hco/7/GRCh38#44385288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6057532-C-A

44385338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6057586-G-A

44385338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6057586-G-T

http://identifiers.org/hco/7/GRCh38#44385379-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6057628-A-C

44385459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6057698-G-T

http://identifiers.org/hco/7/GRCh38#44385489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6057737-C-A

44385514-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6057771-T-A

44385514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6057771-T-C

44385514-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6057771-T-G

44385564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6057817-C-T

http://identifiers.org/hco/7/GRCh38#44385598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6057845-C-A

44385598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6057845-C-T

44385919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6058163-G-A

44385919-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6058163-G-C

44385919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6058163-G-T

44385967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6058201-G-A

44385967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6058201-G-T

44386231-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6058461-G-C

44386231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6058461-G-T

44386267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6058496-G-A

44386267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6058496-G-T

44386318-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6058539-T-A

44386318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6058539-T-C

44386409-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6058632-C-G

44386685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6058880-T-C

44386854-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6059011-C-G

44386874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6059031-T-C

44386937-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6059084-T-G

44387109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6059288-C-T

44388327-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6060206-C-G

44388690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6060469-G-T

44388798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6060557-T-C

44388849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6060606-G-T

http://identifiers.org/hco/7/GRCh38#44389035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6060830-C-A

44389035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6060830-C-T

44389350-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6061105-G-C

44390524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6061740-A-G

44391326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6062340-G-A

44391464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6062465-G-A

44391464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6062465-G-T

44391611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6062589-G-A

44391647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6062613-T-C

44391686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6062642-C-T

44391690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6062646-C-T

44392162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6063114-A-G

44392162-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6063114-A-T

44392423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 6063369-G-A

http://identifiers.org/hco/7/GRCh38#44392528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6063493-C-A

44392528-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6063493-C-G

44392544-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6063545-G-C

44392544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6063545-G-T

44392550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6063551-G-A

44392550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6063551-G-T

44392554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6063555-A-G

44392607-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6063604-G-C

44392607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6063604-G-T

http://identifiers.org/hco/7/GRCh38#44392645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6063643-C-A

44393452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6064272-A-G

44393527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6064355-G-A

44394448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6065316-G-A

http://identifiers.org/hco/7/GRCh38#44394684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6065534-C-A

44394916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6065781-G-A

44394969-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6065840-T-A

44395134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6065978-T-C

44395871-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6067141-C-G

44396089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6067335-G-T

44396908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6067957-A-G

44397060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6068111-A-G

44397171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6068206-C-T

44397225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6068261-C-T

44397366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6068391-G-A

44397366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6068391-G-T

44397385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6068410-C-T

44397408-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6068432-C-G

http://identifiers.org/hco/7/GRCh38#44397424-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6068445-A-C

44398166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6069004-T-C

44398250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6069054-A-G

44398938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6069649-T-C

44399424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6070038-T-C

44399794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6070372-G-A

44399971-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6070565-T-G

http://identifiers.org/hco/7/GRCh38#44400155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6070761-C-A

44400208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6070814-C-T

44400391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6070995-G-A

http://identifiers.org/hco/7/GRCh38#44401081-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6071558-A-C

44401226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6071664-G-A

44401325-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6071763-T-A

44401482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6071909-A-G

44401772-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6072178-C-G

44401773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6072179-T-C

44402196-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6072586-C-G

44402277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6072652-G-A

44402719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6073336-G-A

44402719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6073336-G-T

44402822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6073410-A-G

44402822-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6073410-A-T

http://identifiers.org/hco/7/GRCh38#44402890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6073466-C-A

44403010-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6073550-G-C

44403072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6073611-A-G

44403443-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6074451-G-C

44403449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6074456-G-A

44403985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6074960-A-G

44404144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6075119-G-A

http://identifiers.org/hco/7/GRCh38#44404321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6075307-C-A

44404321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6075307-C-T

44404380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6075358-G-A

44404380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6075358-G-T

44404396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6075374-T-C

44404455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6075433-G-A

44404455-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6075433-G-C

44404482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6075460-A-G

44404524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6075502-C-T

44404541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6075519-G-A

44404697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6075618-A-G

44405537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6077452-A-G

44405566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6077478-G-A

44406349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6078499-T-C

44406590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6078707-T-C

44406590-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6078707-T-G

44406838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6078837-G-A

44406977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6078956-G-A

44406986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6078959-A-G

44407191-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6079120-C-G

44407236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6079165-A-G

44407244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6079173-G-A

http://identifiers.org/hco/7/GRCh38#44407972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6080111-C-A

44407972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6080111-C-T

44407985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6080125-G-A

44408052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6080205-G-A

http://identifiers.org/hco/7/GRCh38#44408065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6080221-C-A

44408404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6080777-A-G

44408616-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6080967-A-T

44409142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6081411-T-C

44409339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6081455-G-A

44409527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6081648-C-T

44414098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6086256-C-T

44414542-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6086640-T-G

44414543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6086641-C-T

http://identifiers.org/hco/7/GRCh38#44414557-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6086655-A-C

44414557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6086655-A-G

44414800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6086977-T-C

44415085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6087271-T-C

44415101-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6087287-T-G

44415232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6087399-A-G

44415359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6087496-C-T

44415380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6087517-T-C

44415380-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6087517-T-G

44415386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6087522-G-A

44415386-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6087522-G-C

44416050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6088109-A-G

44426113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6099133-T-C

44426117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6099135-A-G

44426141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6099159-T-C

44426160-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 6099183-T-A

44426201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6099229-A-G

44426236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6099264-G-T

44426296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6099301-G-A

44426296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6099301-G-T

44426318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6099329-A-G

44426396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6099409-G-A

44426396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6099409-G-T

44427093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6099727-C-T

http://identifiers.org/hco/7/GRCh38#44427350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6100312-C-A

44427428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6100383-T-C

http://identifiers.org/hco/7/GRCh38#44427483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6100423-C-A

44427483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6100423-C-T

http://identifiers.org/hco/7/GRCh38#44427497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6100426-C-A

44427497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6100426-C-T

http://identifiers.org/hco/7/GRCh38#44427514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6100443-C-A

44427557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6100481-G-A

44427557-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6100481-G-C

44427601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6100525-T-C

44427601-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6100525-T-G

44427732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6100647-G-A

44427732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6100647-G-T

44427752-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6100667-G-C

44427752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6100667-G-T

http://identifiers.org/hco/7/GRCh38#44427774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6100682-C-A

44427774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6100682-C-T

44427824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6100722-G-T

http://identifiers.org/hco/7/GRCh38#44427828-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6100726-A-C

44427865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6100761-G-T

44427890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6100786-A-G

44428521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6101037-T-C

44429344-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6102589-T-G

44429395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6102648-A-G

44429474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6102705-T-C

44429674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6102848-T-C

44429700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6102874-G-A

44429787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6102955-T-C

44430077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6103186-G-T

44430264-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6103328-G-C

44430276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6103338-C-T

44430289-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6103351-G-C

http://identifiers.org/hco/7/GRCh38#44430301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6103362-C-A

44430526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6103607-A-G

44430585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6103779-C-T

http://identifiers.org/hco/7/GRCh38#44431523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#6104612-C-A

44431559-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6104643-G-C

http://identifiers.org/hco/7/GRCh38#44432559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6105056-C-A

44432559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6105056-C-T

44433854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6105793-G-A

44434066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6106002-T-C

44434142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6106068-C-T

44437778-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6108277-C-G

44437817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6108336-C-T

http://identifiers.org/hco/7/GRCh38#44438609-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6109526-A-C

44438609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6109526-A-G

44438674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6109587-G-A

http://identifiers.org/hco/7/GRCh38#44438797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6109698-C-A

http://identifiers.org/hco/7/GRCh38#44438885-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6109781-A-C

44438885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6109781-A-G

44438965-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6109836-G-C

44439089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6109957-G-A

44439137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6109975-G-A

44445922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6110369-C-T

44446048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6110493-C-T

44446596-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6110977-C-G

44446621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6110990-G-A

44446666-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6111039-C-G

44446693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6111068-G-A

44446896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6111517-C-T

44447452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6112017-T-C

44447536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6112102-C-T

http://identifiers.org/hco/7/GRCh38#44447698-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6112262-A-C

44448353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6113147-C-T

44448639-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6113403-T-A

44449003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6113734-A-G

44449204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6113904-G-A

44449678-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6114592-A-T

44452038-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6119014-T-G

44452822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6119458-A-G

44453048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6119681-T-C

44453090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6119768-C-T

http://identifiers.org/hco/7/GRCh38#44453225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6119968-C-A

44453225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6119968-C-T

http://identifiers.org/hco/7/GRCh38#44453334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6120064-C-A

44460151-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6122089-T-G

44460155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6122093-C-T

44460222-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6122166-G-C

44460545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6122457-A-G

44460782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6123606-G-A

44460803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6123627-T-C

44461148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6123931-T-C

http://identifiers.org/hco/7/GRCh38#44461175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6123959-C-A

44461272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6124034-G-A

44461301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6124063-A-G

44461486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6124631-G-A

44461486-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6124631-G-C

44462064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6125074-C-T

44462417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6125385-T-C

44462434-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6125406-T-A

44462680-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6125724-C-G

44462902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6125953-C-T

44462907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6125958-C-T

44462951-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6125988-G-C

44466802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6128945-G-T

44466847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6128978-G-A

44466847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6128978-G-T

44467127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6129234-C-T

44467446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6129557-C-T

44471992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6133343-T-C

http://identifiers.org/hco/7/GRCh38#44472047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6133396-C-A

http://identifiers.org/hco/7/GRCh38#44472566-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6133907-A-C

44472812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6134116-G-T

http://identifiers.org/hco/7/GRCh38#44472840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6134143-C-A

44472840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6134143-C-T

44472983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6134273-T-C

44472985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6134275-T-C

44473368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6134647-G-A

44473522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6134800-G-A

44473811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6135077-G-A

http://identifiers.org/hco/7/GRCh38#44473832-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6135097-A-C

44473832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6135097-A-G

44473959-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6135348-C-G

44473959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6135348-C-T

http://identifiers.org/hco/7/GRCh38#44474147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6135521-C-A

44474155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6135529-G-A

44475095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6136151-A-G

44475620-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6136262-C-G

http://identifiers.org/hco/7/GRCh38#44475748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6136371-C-A

44475756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6136379-G-A

http://identifiers.org/hco/7/GRCh38#44475932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6136588-C-A

http://identifiers.org/hco/7/GRCh38#44476107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6136762-C-A

44476204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6136858-G-A

44476204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6136858-G-T

44476335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6136963-A-G

44476396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6137025-C-T

44476794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6137241-C-T

44476857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6137284-T-C

44476859-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6137286-G-C

44476859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6137286-G-T

44477048-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6137434-G-C

44477169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6137554-C-T

44477170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6137555-A-G

44479393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6139201-G-A

44479724-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6139804-A-T

44479803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6139880-G-A

44484942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6143130-G-A

44485030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6143216-T-C

44485157-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6143352-T-A

http://identifiers.org/hco/7/GRCh38#44485225-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6143417-A-C

44485311-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6143550-C-G

44485313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6143695-G-A

44485313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6143695-G-T

44485373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6143754-G-T

44485458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6143825-A-G

44485676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6144196-T-C

44486067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6144667-G-A

44488075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6147301-A-G

44488119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6147353-A-G

44488331-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6147673-T-A

44488395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6147746-G-A

44488395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6147746-G-T

44488413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6147770-A-G

44488415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6147772-G-A

44488756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6148091-T-C

44488756-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6148091-T-G

44488832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6148154-C-T

44488857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6148183-G-A

44489780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6149146-G-A

44489856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6149354-G-A

44489856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6149354-G-T

http://identifiers.org/hco/7/GRCh38#44490091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6149575-C-A

http://identifiers.org/hco/7/GRCh38#44490418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#6149952-C-A

44490418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 6149952-C-T

http://identifiers.org/hco/7/GRCh38#44490586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6150120-C-A

44490586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22208
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6150120-C-T