14490081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3 prime UTR variant
orthologous variants: 91737298-C-T

http://identifiers.org/hco/3/GRCh38#14490129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91737330-C-A

14490129-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3 prime UTR variant
orthologous variants: 91737330-C-G

14490129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3 prime UTR variant
orthologous variants: 91737330-C-T

14490135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3 prime UTR variant
orthologous variants: 91737336-G-A

14490135-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3 prime UTR variant
orthologous variants: 91737336-G-C

14490135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3 prime UTR variant
orthologous variants: 91737336-G-T

14490221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3 prime UTR variant
orthologous variants: 91737416-G-A

14490221-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3 prime UTR variant
orthologous variants: 91737416-G-C

14490221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3 prime UTR variant
orthologous variants: 91737416-G-T

14490257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3 prime UTR variant
orthologous variants: 91737445-T-C

14490318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3 prime UTR variant
orthologous variants: 91737502-A-G

14490335-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3 prime UTR variant
orthologous variants: 91737533-T-A

14490335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3 prime UTR variant
orthologous variants: 91737533-T-C

14490335-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3 prime UTR variant
orthologous variants: 91737533-T-G

14490370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3 prime UTR variant
orthologous variants: 91737567-G-A

14490370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3 prime UTR variant
orthologous variants: 91737567-G-T

http://identifiers.org/hco/3/GRCh38#14490426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91737605-C-A

14490426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3 prime UTR variant
orthologous variants: 91737605-C-T

14490427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3 prime UTR variant
orthologous variants: 91737606-A-G

14490427-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3 prime UTR variant
orthologous variants: 91737606-A-T

14490463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3 prime UTR variant
orthologous variants: 91737647-T-C

14490632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3 prime UTR variant
orthologous variants: 91737784-C-T

http://identifiers.org/hco/3/GRCh38#14490697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91737822-C-A

14490697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3 prime UTR variant
orthologous variants: 91737822-C-T

14490765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3 prime UTR variant
orthologous variants: 91737889-C-T

14490767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3 prime UTR variant
orthologous variants: 91737891-G-A

14490767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3 prime UTR variant
orthologous variants: 91737891-G-T

http://identifiers.org/hco/3/GRCh38#14490775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91737899-C-A

14490775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3 prime UTR variant
orthologous variants: 91737899-C-T

http://identifiers.org/hco/3/GRCh38#14490899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91738004-C-A

http://identifiers.org/hco/3/GRCh38#14490905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91738010-C-A

14490922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3 prime UTR variant
orthologous variants: 91738024-T-C

14491013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3 prime UTR variant
orthologous variants: 91738213-T-C

14491099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 91738426-C-T

14491257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91738586-G-A

14491257-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91738586-G-C

14491257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91738586-G-T

14491288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91738617-G-T

http://identifiers.org/hco/3/GRCh38#14491495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91738810-C-A

14491495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91738810-C-T

14491571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91738890-G-A

14491571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91738890-G-T

http://identifiers.org/hco/3/GRCh38#14491603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91738922-C-A

14491603-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91738922-C-G

14491603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91738922-C-T

14491687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91738990-G-A

14491687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91738990-G-T

14491774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91739072-A-G

http://identifiers.org/hco/3/GRCh38#14491780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91739078-C-A

14491784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91739082-G-A

14491784-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91739082-G-C

14491784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91739082-G-T

14491788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91739087-T-C

14491829-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91739129-C-G

14491829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91739129-C-T

14491973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91739233-A-G

14492007-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91739247-G-T

14492016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91739256-G-T

http://identifiers.org/hco/3/GRCh38#14492043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91739278-C-A

14492043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91739278-C-T

14492070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91739297-T-C

14492086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91739313-G-A

14492086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91739313-G-T

14492125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91739332-G-T

14492300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91739459-G-A

14492300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91739459-G-T

14492349-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91739507-A-T

14492564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91739660-G-A

14492564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91739660-G-T

14492565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91739661-G-T

14492566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91739662-G-A

14492566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91739662-G-T

http://identifiers.org/hco/3/GRCh38#14492611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91739698-C-A

14492611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91739698-C-T

14492643-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91739725-T-A

14492665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91739747-C-T

14492673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91739755-A-G

14492673-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91739755-A-T

14492768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91739841-G-T

14492838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91739880-G-A

14492838-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91739880-G-C

http://identifiers.org/hco/3/GRCh38#14492861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91739896-C-A

14492861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91739896-C-T

14492909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91739918-A-G

http://identifiers.org/hco/3/GRCh38#14493076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91740061-C-A

14493076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91740061-C-T

14493200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91740154-C-T

http://identifiers.org/hco/3/GRCh38#14493219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91740163-C-A

14493333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91740263-G-T

14493370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91740283-T-C

http://identifiers.org/hco/3/GRCh38#14493395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91740307-C-A

14493395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91740307-C-T

http://identifiers.org/hco/3/GRCh38#14493459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91740348-C-A

14493459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91740348-C-T

http://identifiers.org/hco/3/GRCh38#14493465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91740354-C-A

14493465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91740354-C-T

14493468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91740357-C-T

14493555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91740373-G-A

14493555-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91740373-G-C

14493555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91740373-G-T

http://identifiers.org/hco/3/GRCh38#14493561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91740378-C-A

14493561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91740378-C-T

14493574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91740390-G-T

14493660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91740424-T-C

14493790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 91740551-G-A

14493818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 91740579-G-A

http://identifiers.org/hco/3/GRCh38#14493843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91740604-C-A

14493843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91740604-C-T

14494322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91741288-G-A

14494411-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91741364-G-C

14494609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91741539-C-T

14494768-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91741630-G-C

14494768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91741630-G-T

14494891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 91741725-A-G

14494927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 91741761-C-T

14495035-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91741850-C-G

14495035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91741850-C-T

14495036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91741851-C-T

http://identifiers.org/hco/3/GRCh38#14495082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91741887-C-A

http://identifiers.org/hco/3/GRCh38#14495117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91741919-C-A

14495117-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91741919-C-G

14495117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91741919-C-T

14496522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 91742334-G-A

14496574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91742385-G-A

14496574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91742385-G-T

14496592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91742401-T-C

http://identifiers.org/hco/3/GRCh38#14496624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91742436-C-A

14496654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91742450-A-G

14496680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91742472-T-C

14496680-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91742472-T-G

http://identifiers.org/hco/3/GRCh38#14496684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91742476-C-A

14496684-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91742476-C-G

14496800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91742565-G-A

14497741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91743004-G-A

14497757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91743023-T-C

http://identifiers.org/hco/3/GRCh38#14498014-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91743197-A-C

14498051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91743235-C-T

14498950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91744698-A-G

14499069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91744785-G-A

14499069-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91744785-G-C

14499359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91745025-T-C

http://identifiers.org/hco/3/GRCh38#14503420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91748885-C-A

14503420-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91748885-C-G

14503420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91748885-C-T

http://identifiers.org/hco/3/GRCh38#14503438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91748903-C-A

14503467-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91749523-T-G

http://identifiers.org/hco/3/GRCh38#14503485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91749543-C-A

14503485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91749543-C-T

http://identifiers.org/hco/3/GRCh38#14503512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91749562-C-A

14503512-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91749562-C-G

14503512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91749562-C-T

14503546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91749594-T-C

14503631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 91749679-T-C

14503659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 91749707-G-T

14503720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 91749764-G-A

14503720-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 91749764-G-C

14503720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 91749764-G-T

14503724-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 91749768-T-A

14503724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 91749768-T-C

14503724-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 91749768-T-G

14503803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 91749845-G-A

14503803-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 91749845-G-C

14503803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 91749845-G-T

http://identifiers.org/hco/3/GRCh38#14503808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91749850-C-A

14503808-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 91749850-C-G

14503808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 91749850-C-T

14503823-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 91749865-T-G

14503847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 91749889-G-A

14503847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 91749889-G-T

14504025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91750073-G-A

14504025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91750073-G-T

14504032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91750080-G-A

14504032-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91750080-G-C

14504032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91750080-G-T

14504056-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91750104-T-A

14504057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91750105-G-A

14504057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91750105-G-T

http://identifiers.org/hco/3/GRCh38#14504073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91750120-C-A

14504073-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91750120-C-G

http://identifiers.org/hco/3/GRCh38#14504094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91750141-C-A

http://identifiers.org/hco/3/GRCh38#14504147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91750193-C-A

14504147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91750193-C-T

14505206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91750406-G-A

http://identifiers.org/hco/3/GRCh38#14505217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91750420-C-A

14505217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91750420-C-T

14505231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91750444-G-A

14505232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91750445-G-A

14505381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91750584-G-A

http://identifiers.org/hco/3/GRCh38#14505482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91750663-C-A

http://identifiers.org/hco/3/GRCh38#14505585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91750743-C-A

14505585-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91750743-C-G

14505598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91750757-G-A

http://identifiers.org/hco/3/GRCh38#14505692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91750845-C-A

14505692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 91750845-C-T

http://identifiers.org/hco/3/GRCh38#14505811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91750964-C-A

14505898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91751042-T-C

14505898-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91751042-T-G

14505899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91751043-G-T

14505904-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91751048-T-A

14505904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91751048-T-C

14505992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91751129-G-A

14506032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91751154-C-T

14506109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91751208-G-A

14506345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91751348-C-T

14506347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91751350-T-C

14506448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91751412-A-G

http://identifiers.org/hco/3/GRCh38#14506701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91751602-C-A

14506701-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91751602-C-G

14506701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91751602-C-T

14506804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 91751666-G-A

14506804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 91751666-G-T

http://identifiers.org/hco/3/GRCh38#14506820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91751682-C-A

14506820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 91751682-C-T

14506972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 91751834-G-A

14506972-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 91751834-G-C

14506972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 91751834-G-T

http://identifiers.org/hco/3/GRCh38#14507035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91751900-C-A

14507035-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91751900-C-G

14507035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91751900-C-T

http://identifiers.org/hco/3/GRCh38#14507036-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91751901-A-C

14507036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91751901-A-G

14507059-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91751916-T-G

http://identifiers.org/hco/3/GRCh38#14507111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91751969-C-A

14507111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91751969-C-T

http://identifiers.org/hco/3/GRCh38#14507135-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91751989-A-C

14507316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91752112-G-A

14507426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 91752220-T-C

http://identifiers.org/hco/3/GRCh38#14507494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91752264-C-A

14507494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91752264-C-T

14507506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91752273-G-A

14507506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91752273-G-T

14507655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 91752420-G-A

14507655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 91752420-G-T

http://identifiers.org/hco/3/GRCh38#14507682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91752447-C-A

14507754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91752520-G-A

14507771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91752537-G-T

14507793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91752560-G-T

14508883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91753542-G-A

14508893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91753552-A-G

http://identifiers.org/hco/3/GRCh38#14508990-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#91753614-A-C

14508991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 91753615-G-A

http://identifiers.org/hco/3/GRCh38#14509035-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#91753631-A-C

http://identifiers.org/hco/3/GRCh38#14509078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#91753672-C-A

14509204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91753752-C-T

14509278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91753803-G-T

14509473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91753981-G-A

14509473-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91753981-G-C

14509650-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91754179-T-A

14509650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91754179-T-C

14509778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91754303-T-C

14509795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91754320-G-T

http://identifiers.org/hco/3/GRCh38#14509800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91754326-C-A

14509800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91754326-C-T

http://identifiers.org/hco/3/GRCh38#14509945-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91754471-A-C

14509945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 91754471-A-G

14509945-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 91754471-A-T

14509979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91754507-A-G

14509979-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91754507-A-T

http://identifiers.org/hco/3/GRCh38#14510093-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91754607-A-C

14510095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91754609-G-T

14511596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 91755974-C-T

14511672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 91756056-G-A

14512765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91756104-G-A

14512811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 91756150-C-T

14512834-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91756173-T-G

http://identifiers.org/hco/3/GRCh38#14512923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91756267-C-A

14512931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 91756275-T-C

14512950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 91756294-G-A

14512950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 91756294-G-T

14512970-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 91756317-T-A

14512970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 91756317-T-C

14513461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 91756678-C-T

14513636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 91756781-T-C

http://identifiers.org/hco/3/GRCh38#14513663-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: NMD_transcript_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91756803-A-C

14513699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 91756839-G-A

14513699-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91756839-G-C

14513708-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 91756848-T-A

14513708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 91756848-T-C

14513708-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 91756848-T-G

14513750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 91756890-G-A

14513750-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91756890-G-C

14513750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91756890-G-T

14513898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91757021-G-A

14513898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91757021-G-T

http://identifiers.org/hco/3/GRCh38#14513936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91757050-C-A

14513936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91757050-C-T

http://identifiers.org/hco/3/GRCh38#14514184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91757196-C-A

14514184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91757196-C-T

http://identifiers.org/hco/3/GRCh38#14514208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91757220-C-A

14514208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91757220-C-T

14514283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91757303-G-A

http://identifiers.org/hco/3/GRCh38#14514369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91757389-C-A

14514378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 91757398-G-T

14514396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 91757416-G-A

14514396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 91757416-G-T

14514526-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91757543-T-A

http://identifiers.org/hco/3/GRCh38#14514550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91757562-C-A

14514576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91757592-G-T

14514586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91757602-G-T

14514597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91757613-G-T

14514606-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91757622-T-A

14517019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91759258-A-G

14517019-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91759258-A-T

14517020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91759259-G-A

14517020-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91759259-G-C

14517020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91759259-G-T

14517032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91759271-G-A

14517032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91759271-G-T

14517038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91759277-G-A

14517038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91759277-G-T

14517173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 91759400-G-A

14517212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 91759439-G-A

http://identifiers.org/hco/3/GRCh38#14517300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91759526-C-A

14517300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91759526-C-T

14517317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91759545-G-A

14517317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91759545-G-T

14517320-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91759548-T-A

14517333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91759562-T-C

14517698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91759696-T-C

14517762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91759754-G-A

14517762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91759754-G-T

http://identifiers.org/hco/3/GRCh38#14517908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91759896-C-A

14517908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91759896-C-T

14517946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91759933-G-A

14517946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91759933-G-T

14517947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91759934-A-G

14518046-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91760037-T-A

14518046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91760037-T-C

14518208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91760129-A-G

14520561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91760986-T-C

http://identifiers.org/hco/3/GRCh38#14520592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91761016-C-A

14520592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91761016-C-T

14520593-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91761017-A-T

14520745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91761058-G-A

14520745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91761058-G-T

http://identifiers.org/hco/3/GRCh38#14520953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91761089-C-A

http://identifiers.org/hco/3/GRCh38#14521063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91761177-C-A

http://identifiers.org/hco/3/GRCh38#14521177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91761291-C-A

14521177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91761291-C-T

14521377-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91761462-T-G

http://identifiers.org/hco/3/GRCh38#14521402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91761483-C-A

14521402-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91761483-C-G

14521402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91761483-C-T

http://identifiers.org/hco/3/GRCh38#14521569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91761620-C-A

14521569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91761620-C-T

http://identifiers.org/hco/3/GRCh38#14522096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91761938-C-A

14522096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91761938-C-T

14522143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91761956-A-G

14522197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91762014-G-A

14522197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91762014-G-T

14522219-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91762037-T-G

http://identifiers.org/hco/3/GRCh38#14522292-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91762104-A-C

14522539-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91762339-T-A

http://identifiers.org/hco/3/GRCh38#14522541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91762341-C-A

14522543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91762343-T-C

http://identifiers.org/hco/3/GRCh38#14522618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91762379-C-A

14522618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91762379-C-T

http://identifiers.org/hco/3/GRCh38#14522640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91762399-C-A

14522640-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91762399-C-G

14522819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91762492-T-C

http://identifiers.org/hco/3/GRCh38#14522892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91762539-C-A

14522892-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91762539-C-G

14522916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91762576-G-T

14523245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91762834-G-T

14523278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91762867-C-T

http://identifiers.org/hco/3/GRCh38#14523320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91762915-C-A

14523320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91762915-C-T

14523332-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91762927-T-G

http://identifiers.org/hco/3/GRCh38#14523426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91763003-C-A

http://identifiers.org/hco/3/GRCh38#14523436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91763013-C-A

14523436-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91763013-C-G

http://identifiers.org/hco/3/GRCh38#14523444-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91763021-A-C

14523454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91763031-A-G

14523457-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91763034-T-A

14523460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91763037-T-C

14523502-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91763295-T-A

14523502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91763295-T-C

14523502-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91763295-T-G

14523510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91763303-G-A

14523510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91763303-G-T

14523517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91763310-A-G

14523517-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91763310-A-T

14523658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 91763494-G-A

http://identifiers.org/hco/3/GRCh38#14523694-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91763530-A-C

14523694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 91763530-A-G

14523711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91763547-G-A

14523711-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91763547-G-C

14523711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91763547-G-T

14523797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91763636-C-T

http://identifiers.org/hco/3/GRCh38#14523842-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91763680-A-C

14523848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91763686-G-A

http://identifiers.org/hco/3/GRCh38#14523863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91763701-C-A

14523863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91763701-C-T

http://identifiers.org/hco/3/GRCh38#14523943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91763758-C-A

14523971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91763776-A-G

http://identifiers.org/hco/3/GRCh38#14524041-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91763846-A-C

14524041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91763846-A-G

14524041-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91763846-A-T

http://identifiers.org/hco/3/GRCh38#14524056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91763861-C-A

14524086-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91763889-G-C

14524086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91763889-G-T

http://identifiers.org/hco/3/GRCh38#14524137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91763940-C-A

14524137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91763940-C-T

http://identifiers.org/hco/3/GRCh38#14524140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91763943-C-A

14524277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91764044-C-T

http://identifiers.org/hco/3/GRCh38#14524466-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91764238-A-C

14524466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 91764238-A-G

14524466-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91764238-A-T

14524561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91764333-C-T

14524576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91764347-G-A

http://identifiers.org/hco/3/GRCh38#14524591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91764360-C-A

http://identifiers.org/hco/3/GRCh38#14524674-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91764413-A-C

14524674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91764413-A-G

14524700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91764439-C-T

14524843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91764599-C-T

14524880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91764629-C-T

14524997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91764689-G-A

14525090-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91764748-T-A

14525090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91764748-T-C

http://identifiers.org/hco/3/GRCh38#14525340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91764958-C-A

14525383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91764975-C-T

14525384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91764976-C-T

14525454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 91765006-A-G

14525514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 91765066-G-A

14525514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 91765066-G-T

14525599-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91765145-G-C

14525602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91765148-C-T

14525667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91765201-G-A

14525667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91765201-G-T

14525671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91765205-C-T

14525676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91765210-C-T

14525760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91765267-G-T

http://identifiers.org/hco/3/GRCh38#14525774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91765281-C-A

14525774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91765281-C-T

14525817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91765312-G-A

14525817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91765312-G-T

14525842-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91765334-C-G

14525842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91765334-C-T

14525906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 91765400-G-A

14525906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 91765400-G-T

14525948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91765447-G-A

14525948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91765447-G-T

14525966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91765474-C-T

14526001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91765512-G-A

http://identifiers.org/hco/3/GRCh38#14526064-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91765521-C-A

14526064-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91765521-C-G

14526064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91765521-C-T

http://identifiers.org/hco/3/GRCh38#14526094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91765547-C-A

14526094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91765547-C-T

14526159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91765582-C-T

14526177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91765600-G-A

14526184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91765607-T-C

14526249-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91765680-G-C

http://identifiers.org/hco/3/GRCh38#14526318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91765751-C-A

http://identifiers.org/hco/3/GRCh38#14526345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91765777-C-A

14526368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91765800-A-G

14526385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91765817-G-T

http://identifiers.org/hco/3/GRCh38#14526494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91765912-C-A

http://identifiers.org/hco/3/GRCh38#14526647-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91766048-A-C

http://identifiers.org/hco/3/GRCh38#14526716-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91766106-A-C

14531670-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91767315-T-G

14531932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91767509-G-A

14532333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91767789-G-A

http://identifiers.org/hco/3/GRCh38#14532335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91767791-C-A

14532335-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91767791-C-G

14532343-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91767798-G-C

14532373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91767823-G-A

14532458-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91767861-G-C

14532584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91767980-T-C

14532840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91768032-A-G

14532847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91768039-G-A

14532985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91768163-T-C

14533134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91768335-C-T

14533174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91768375-C-T

14533262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91768460-T-C

14533345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91768540-A-G

14533345-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91768540-A-T

14533416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91768604-G-A

14533416-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91768604-G-C

14533416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91768604-G-T

14534145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91769090-C-T

14534187-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91769134-G-C

14534224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91769172-A-G

14534352-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91769280-G-C

14534352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91769280-G-T

http://identifiers.org/hco/3/GRCh38#14534487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91769444-C-A

14534752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91769654-G-A

14534752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91769654-G-T

14534757-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91769659-G-C

14534936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91769832-G-T

14537227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91771015-C-T

14537234-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91771020-C-G

14537315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91771101-G-A

14537406-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91771183-T-G

14537632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91771349-C-T

14537744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91771453-T-C

14537763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91771461-C-T

14537825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91771523-G-A

14537899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91771597-G-A

14538388-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91772012-C-G

14538420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91772019-C-T

14538462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91772055-G-A

14539683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91772751-C-T

14540205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91773148-G-A

http://identifiers.org/hco/3/GRCh38#14540255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91773172-C-A

14540255-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91773172-C-G

14540334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 91773242-C-T

14540390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 91773292-G-A

14540390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 91773292-G-T

http://identifiers.org/hco/3/GRCh38#14540405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91773301-C-A

14540405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91773301-C-T

14540471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91773359-G-A

14540471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91773359-G-T

14540523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91773404-C-T

http://identifiers.org/hco/3/GRCh38#14540562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91773468-C-A

14540587-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91773492-C-G

http://identifiers.org/hco/3/GRCh38#14540847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91773724-C-A

14540862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91773737-A-G

14540878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91773751-C-T

http://identifiers.org/hco/3/GRCh38#14541074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91773947-C-A

14541160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91774034-C-T

14541163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91774037-G-A

14541363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91774222-G-A

14541452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91774249-G-A

http://identifiers.org/hco/3/GRCh38#14541514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91774263-C-A

14541654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91774349-C-T

14541711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91774397-G-A

http://identifiers.org/hco/3/GRCh38#14541742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91774427-C-A

14541989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 91774637-A-G

14542774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91775030-T-C

14542794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91775049-T-C

14542856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91775101-C-T

14542967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91775165-G-A

14543088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91775275-C-T

14543098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91775279-C-T

14543254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91775408-C-T

14543264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91775418-C-T

14543265-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91775419-G-C

14543484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91775573-G-A

14543484-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91775573-G-C

14543489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91775580-C-T

14543579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91775630-T-C

14543800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91775818-G-A

14543952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91775941-G-A

14544149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91776379-G-A

14544151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91776381-G-T

14544523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91776742-C-T

14544534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91776753-A-G

14544702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91776913-C-T

14544878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91777046-C-T

14545616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91777303-G-A

14547734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91778332-T-C

14547865-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91778418-A-T

14548021-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91778541-C-G

14548123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91778566-G-A

14548267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91778688-C-T

14548364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91778779-G-A

14548593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91778930-C-T

http://identifiers.org/hco/3/GRCh38#14548703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91779081-C-A

14548750-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91779137-G-C

14548814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91779196-A-G

14548976-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91779352-T-A

14549421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91779652-T-C

14549490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91779721-G-A

14549490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91779721-G-T

14550256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91780466-C-T

14550342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91780540-T-C

14550362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91780552-T-C

14550677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91780805-G-A

14550800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91780919-C-T

14550909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91781006-C-T

14551060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91781152-G-A

14551284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91781371-G-A

14551458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91781561-C-T

14551540-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91781619-G-C

14551707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91781779-G-A

14551757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91781829-G-A

14551792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91781863-G-A

14551840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91781907-G-A

14552060-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91782119-T-A

14552160-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91782178-C-G

14552160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91782178-C-T

14552211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91782242-C-T

14552445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91782429-A-G

14552495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91782469-C-T

http://identifiers.org/hco/3/GRCh38#14554668-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91783108-A-C

14554784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91783201-C-T

http://identifiers.org/hco/3/GRCh38#14554853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91783261-C-A

14554854-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91783262-C-G

14554863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91783271-G-A

14554863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91783271-G-T

14554954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91783350-T-C

14555069-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91783466-T-G

http://identifiers.org/hco/3/GRCh38#14555106-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91783511-A-C

14555131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91783539-G-A

14555132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91783540-A-G

14555346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91783763-G-A

14555505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91783893-G-A

http://identifiers.org/hco/3/GRCh38#14555788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91784139-C-A

14555788-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91784139-C-G

http://identifiers.org/hco/3/GRCh38#14555789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91784140-C-A

14555789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91784140-C-T

http://identifiers.org/hco/3/GRCh38#14555790-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91784141-A-C

14555790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91784141-A-G

14555825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91784172-G-T

http://identifiers.org/hco/3/GRCh38#14555839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91784186-C-A

14555839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91784186-C-T

http://identifiers.org/hco/3/GRCh38#14555869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91784209-C-A

14555869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91784209-C-T

http://identifiers.org/hco/3/GRCh38#14555877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91784219-C-A

14555877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91784219-C-T

14556003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91784367-C-T

http://identifiers.org/hco/3/GRCh38#14556010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91784373-C-A

14556010-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91784373-C-G

14556170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron variant
orthologous variants: 91784512-G-A

14556231-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron variant
orthologous variants: 91784577-C-G

14556231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron variant
orthologous variants: 91784577-C-T

14557505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron variant
orthologous variants: 91785561-A-G

14557639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron variant
orthologous variants: 91785700-C-T

14558203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron variant
orthologous variants: 91786311-A-G

14558252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron variant
orthologous variants: 91786361-C-T

14558268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron variant
orthologous variants: 91786372-C-T

14558288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23841
most severe consequence: intron variant
orthologous variants: 91786392-A-G