141923903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38383385-C-T

141924002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38383480-T-C

141924009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38383487-C-T

141924019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38383497-G-A

141924019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38383497-G-T

141924037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38383516-G-A

141924037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38383516-G-T

141924041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38383521-G-A

141924041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38383521-G-T

http://identifiers.org/hco/5/GRCh38#141924088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38383568-C-A

141924088-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38383568-C-G

141924088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38383568-C-T

141924112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38383599-G-T

141924121-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38383608-T-A

141924121-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38383608-T-G

141924163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38383650-G-A

141924606-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38384164-C-G

141925422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38384348-T-C

141925428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38384354-A-G

141925509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38384435-A-G

141925656-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38384554-G-C

141925656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38384554-G-T

141925657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38384555-G-A

141925657-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38384555-G-C

141925703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38384601-A-G

141927803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38385567-A-G

141928000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38385739-A-G

141928042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38385783-G-A

141928137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38385858-G-A

141928153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 38385876-C-T

141928162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38385885-C-T

141928239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38385959-G-A

141928292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38386012-T-C

http://identifiers.org/hco/5/GRCh38#141928404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38386127-C-A

141928404-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38386127-C-G

141928404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38386127-C-T

http://identifiers.org/hco/5/GRCh38#141928446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38386167-C-A

141928446-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38386167-C-G

141928446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38386167-C-T

http://identifiers.org/hco/5/GRCh38#141928601-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38386321-A-C

141928779-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38386488-C-G

141928860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38386569-A-G

141929002-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38386707-G-C

141929072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38386769-G-A

141929608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38386987-C-T

141929756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38387138-A-G

141929799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38387162-A-G

141929969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38387313-T-C

141929976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38387320-C-T

141930030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38387374-G-A

141930116-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38387463-C-G

141930180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 38387525-A-G

http://identifiers.org/hco/5/GRCh38#141930288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38387629-C-A

141930288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38387629-C-T

141930368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38387701-A-G

http://identifiers.org/hco/5/GRCh38#141930369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38387702-C-A

141930369-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38387702-C-G

141930369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38387702-C-T

141930523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38387856-C-T

141930735-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38388128-T-A

http://identifiers.org/hco/5/GRCh38#141930921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38388312-C-A

141931100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38388648-G-A

141931137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38388682-C-T

141931178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38388726-T-C

141931213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38388758-G-T

http://identifiers.org/hco/5/GRCh38#141931229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38388774-C-A

141931229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38388774-C-T

141931262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38388807-C-T

141931266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38388810-A-G

141931287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 38388831-G-A

141931287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 38388831-G-T

141931415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38388957-T-C

141931418-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38388960-T-A

141931464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38388995-T-C

141931693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38389173-G-A

141931729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38389208-C-T

141932306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38389723-G-A

141932364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38389777-A-G

141932364-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38389777-A-T

141932375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38389788-T-C

141932588-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38389980-T-G

141932597-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38389998-G-C

141932729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38390079-G-T

141932730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38390080-G-A

141933090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38390201-A-G

http://identifiers.org/hco/5/GRCh38#141933196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38390250-C-A

141933406-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38390458-T-A

141933406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38390458-T-C

141933479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38390503-T-C

141933510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38390534-G-T

141933511-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38390535-G-C

141933511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38390535-G-T

141933590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38390619-A-G

141933631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38390643-A-G

141933644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38390656-G-A

141933683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38390691-A-G

http://identifiers.org/hco/5/GRCh38#141933743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38390766-C-A

141934089-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38390951-T-G

141934180-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38391032-T-A

141934180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38391032-T-C

141934180-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38391032-T-G

141934247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38391088-T-C

141934258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 38391099-T-C

141934266-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38391107-C-G

141934266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38391107-C-T

141934267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38391108-A-G

141934432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38391264-C-T

141934435-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38391267-A-T

141934579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38391408-A-G

141934579-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38391408-A-T

141934624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38391456-G-A

http://identifiers.org/hco/5/GRCh38#141934700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38391529-C-A

http://identifiers.org/hco/5/GRCh38#141934705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38391534-C-A

141934705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38391534-C-T

141934865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38391692-G-A

141934865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38391692-G-T

141934869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38391696-T-C

141934897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38391727-A-G

141934897-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38391727-A-T

141934900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38391730-T-C

http://identifiers.org/hco/5/GRCh38#141934938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38391766-C-A

141934953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38391781-G-A

141934953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38391781-G-T

141934973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38391800-A-G

141934993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38391820-A-G

http://identifiers.org/hco/5/GRCh38#141935000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38391834-C-A

141935000-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38391834-C-G

141935000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38391834-C-T

141935001-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38391835-A-T

141935005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38391839-G-T

141935016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38391850-G-A

141935016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38391850-G-T

141935047-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38391871-T-A

141935047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38391871-T-C

141935047-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38391871-T-G

141935209-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38391974-G-C

141935209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38391974-G-T

141935293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38392057-G-A

141935458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38392216-T-C

http://identifiers.org/hco/5/GRCh38#141935510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38392265-C-A

141936985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38392791-G-A

141936985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38392791-G-T

141936994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38392800-T-C

141937014-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 38392813-G-C

141937014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 38392813-G-T

141937026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38392825-G-A

141937064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38392862-G-A

141937126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38392900-C-T

141937200-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 38392952-C-G

141937278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 38393030-A-G

141937278-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38393030-A-T

141937318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 38393070-C-T

141937319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38393071-A-G

141937395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38393139-G-T

141937429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38393168-A-G

141937437-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38393176-C-G

141937470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38393209-G-A

141937470-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38393209-G-T

http://identifiers.org/hco/5/GRCh38#141937483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38393222-C-A

141937483-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38393222-C-G

141937483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38393222-C-T

141938355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38393581-C-T

141938369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38393595-C-T

http://identifiers.org/hco/5/GRCh38#141938389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38393615-C-A

141938389-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38393615-C-G

141938389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38393615-C-T

http://identifiers.org/hco/5/GRCh38#141938393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38393619-C-A

141938393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38393619-C-T

141938409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38393635-G-A

141938409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38393635-G-T

141938501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38394091-G-T

141938549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38394139-A-G

141938606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38394196-A-G

http://identifiers.org/hco/5/GRCh38#141938633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38394223-C-A

141938646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38394236-G-A

141938657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38394247-C-T

141938672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38394262-C-T

141938735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38394313-T-C

141938738-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38394316-T-A

141938763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38394341-G-A

141938763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38394341-G-T

141938764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38394342-A-G

141938767-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 38394345-T-A

141938812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38394395-G-A

141938830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38394413-G-T

141938873-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38394454-C-G

141938873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38394454-C-T

141938907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38394487-A-G

141938916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38394497-A-G

141938917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38394498-T-C

141938930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38394511-T-C

141938944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38394533-G-T

141938947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38394536-G-T

141938998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38394563-T-C

141939082-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38394625-C-G

141939084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38394627-T-C

141939113-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38394652-A-T

141939131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38394669-G-A

141939131-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38394669-G-C

http://identifiers.org/hco/5/GRCh38#141939639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38395008-C-A

141939664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38395033-G-A

141939700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38395068-G-A

141939700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38395068-G-T

141939705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38395073-G-A

141939732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38395084-T-C

http://identifiers.org/hco/5/GRCh38#141939742-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38395094-A-C

141939742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38395094-A-G

http://identifiers.org/hco/5/GRCh38#141939810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38395147-C-A

141939810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38395147-C-T

141939838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38395175-G-A

141939838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38395175-G-T

141939913-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38395451-T-G

http://identifiers.org/hco/5/GRCh38#141939947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38395489-C-A

http://identifiers.org/hco/5/GRCh38#141940155-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38395684-A-C

141940155-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38395684-A-T

141940409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38395934-G-A

141940409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38395934-G-T

141940412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38395937-G-A

141940412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38395937-G-T

141940425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38395950-A-G

141940430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38395959-G-A

141940698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38396217-A-G

141940819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38396317-A-G

141940869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38396366-A-G

141940880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38396382-G-T

141940919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38396421-G-T

http://identifiers.org/hco/5/GRCh38#141940942-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38396444-C-A

141940942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38396444-C-T

141940979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38396479-T-C

141941156-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38396594-T-A

141941156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38396594-T-C

141941225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38396650-G-A

141941393-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38396778-A-T

141941394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38396779-G-A

141941394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38396779-G-T

http://identifiers.org/hco/5/GRCh38#141941421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38396801-C-A

141941421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38396801-C-T

141941510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38396888-T-C

141941548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38396920-G-A

141941548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38396920-G-T

141941552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38396924-C-T

141941614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38396995-G-A

141941614-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38396995-G-C

141941614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38396995-G-T

141941635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38397028-G-A

141941635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38397028-G-T

http://identifiers.org/hco/5/GRCh38#141941643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38397036-C-A

141941731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38397103-A-G

141941845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38397205-A-G

141941852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28969
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38397212-G-A